Halogenation of arenes using alkali metal halides/Fe(NO3)3·9H2O at room temperature

TL;DR

A new, eco-friendly method for halogenating arenes using iron nitrate and alkali metal halides at room temperature was developed.

Contribution

The method enables efficient halodecarboxylation of anisole analogues at room temperature using Fe(NO3)3·9H2O and alkali metal halides.

Findings

Electron-donating substrates gave good to excellent yields.

Electron-withdrawing substrates gave low to moderate yields.

The method works for gram-scale synthesis.

Abstract

A simple, efficient and environmentally friendly methodology for the halodecarboxylation of anisole analogues using Fe(NO3)3·9H2O/KBr or NaI at room temperature was developed. In this method, most substrates with an electron-donating group afforded corresponding products in good to excellent yields, whereas those with an electron-withdrawing group afforded low to moderate yields. More importantly, this protocol was also applicable for gram-scale synthesis. It is hoped that this methodology will be highly useful in organic synthesis.

A simple, efficient and environmentally friendly methodology for the halodecarboxylation of anisole analogues using Fe(NO3)3·9H2O/KBr or NaI at room temperature was developed.

Figures

Scale-up of bromination by Fe(NO3)3·9H2O/KBr.

Possible mechanisms for bromination.

Tables

Table 1. Optimization of reaction conditionsa

Entry	Salt	Br-source	T/h	Solvent	Yield (%)
1	Fe(NO3)3·9H2O	KBr	2 h	H2O	7
2	Fe(NO3)3·9H2O	KBr	2 h	DMSO	9
3	Fe(NO3)3·9H2O	KBr	2 h	Acetone	<1
4	Fe(NO3)3·9H2O	KBr	2 h	DMF	3
5	Fe(NO3)3·9H2O	KBr	2 h	NMP	<1
6	Fe(NO3)3·9H2O	KBr	2 h	Hexane	67
7	Fe(NO3)3·9H2O	KBr	2 h	CH2Cl2	98
8	Fe(NO3)3·9H2O	KBr	2 h	EA	87
9	Fe(NO3)3·9H2O	KBr	2 h	Methanol	<1
10	Fe(NO3)3·9H2O	KBr	2 h	Ethanol	3
11	Fe(NO 3 ) 3 ·9H 2 O	KBr	2 h	CH 3 CN	>99
12	Fe(NO3)3·9H2O	NaBr	2 h	CH3CN	98
13	Fe(NO3)3·9H2O	LiBr	2 h	CH3CN	95
14	Fe(NO3)3·9H2O	CuBr2	2 h	CH3CN	96b
15	Fe(NO3)3·9H2O	FeBr3	2 h	CH3CN	95c
16	Fe(NO3)3·9H2O	KBr	1 h	CH3CN	57
17	Fe(NO3)3·9H2O	KBr	3 h	CH3CN	97
18	Fe(NO3)3·9H2O	KBr	4 h	CH3CN	96
19	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	95d
20	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	94e
21	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	92f
22	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	29g
23	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	65h
24	Fe(NO3)3·9H2O	KBr	2 h	CH3CN	64i
25	—	KBr	2 h	CH3CN	<1
26	FeCl3	KBr	2 h	CH3CN	<1
27	FeBr3	KBr	2 h	CH3CN	<1
28	Fe2(SO4)3	KBr	2 h	CH3CN	<1
29	Cu(NO3)2	KBr	2 h	CH3CN	29
30	Co(NO3)2	KBr	2 h	CH3CN	<1
31	Ce(NO3)3·6H2O	KBr	2 h	CH3CN	<1

Table 2. Bromination of various substratesa

Entry	Substrate	Product	Yield/%
1			>99
2			96
3			90
4			83
5			89
6			85/99b
7			97
8			86c
9			71/91b
10			98
11			99
12			98
13			97
14			61/93b
15			79/96b
16			77/91c
17			50/96b
18			64/96b
19			6/68b
20			<1
21			<1
22			72/15
			94d/5d
23			>99e
24			84
25			82
26			79
27			90f
28			33/65b
29			<1
30			87

Table 3. Iodination of various substratesa

Entry	Substrate	Product	Yield/%
1			>99
2			>99
3			>99
4			>99
5			>99
6			90
7			98
8			99
9			35b
10			<1
11			73
			26
12			94
13			93
14			41/69b

Table 4. Quenching experiments for the bromination process

Additive	Equiv.	Yield of 1 (%)	Yield of 2 (%)
TEMPO	0	72	16
TEMPO	0.5	69	2
TEMPO	0.25	60	13
BHT	0.25	72	7

Full text

Introduction

Aryl halides are very common structural units widely present in a large number of natural products, industrial chemicals and pharmaceuticals.^1^ Additionally, aryl halides are important synthetic blocks to construct various compounds.^2^ A series of cross-coupling reactions including the Heck reaction, Suzuki reaction, Ullmann reaction, Grignard reaction, Stille reaction, Sonogashira reaction, Negishi reaction, Kumada reaction, and Hiyama reaction can be conducted using aryl halides.

However, hazardous, toxic and corrosive molecular halogens are usually used as halogenating agents in the laboratory,^3^e.g., in bromination, where bromine is used as a direct reagent for the synthesis of bromoaromatic compounds, which causes environmental pollution and some undesirable side reactions such as the production of toxic HBr gas, uncontrolled polybromination and lower yields. Thus, many reagents have been developed to replace molecular halogens as the source of electrophilic halide cations. The most common alternative to Br_2_ is NBS,^4^ which is used as a “Br” source via electrophilic substitution to obtain brominated compounds, which is an important way to produce bromides. Essentially, bromide anions were reacted with oxidants to generate Br^+^. Further, co-oxidants such as PhI(OAc)2,^5^ H_2_O_2_ (ref. 6) and metal oxidants^7^ were developed. Meanwhile, quaternary ammonium salts,^8^ pyridinium salts,^9^ 4-(dimethylamino)pyridine tribromide^10^ and N,N-dibromotosylamide (TsNBr_2_)^11^ were selected as bromination reagents. In recent years, Lewis or Brønsted acids and Lewis bases have been employed to boost the reactivity of bromination by different research groups.^12^ Nevertheless, most of these methods suffer from limitations such as the requirement for essential transition-metal catalysts, inevitable operational complexity, uncommon bromine sources, and a narrow substrate range. Therefore, efficient preparation of aryl halides under mild and green reaction conditions is a continuing goal for chemists in organic synthesis and several other research fields.

In recent years, considerable attention has been paid to the development of a new route for the construction of halogenated scaffolds by utilizing safe and readily available halide sources such as alkali metal halides (halide = I, Br, and Cl).^13^ A combination of oxidants and bromides such as oxone/NaBr,^14^ CAN/KBr,^15^ CAN/LiBr,^16^ Selectfluor®/KBr,^17^ NaBrO_3_–NaBr,^18^ and NaBr/NaNO_3_/TFA^19^ has been employed in these bromination reactions. We also noted that Fe(NO_3_)3·9H_2_O had relatively high Lewis acidity and great catalytic activity.^20^ Meanwhile, Fe(NO_3_)3·9H_2_O is a cheap, non-toxic and readily available inorganic oxidant and has been used as an efficient oxidant,^21^ nitro source^22^ and catalyst in cross-coupling reactions.^23^ We also found that I_2_ could be generated in situ from Fe(NO_3_)3·9H_2_O/NaI in DMSO to catalyze the oxidation process.^24^ Thus, we propose that Fe(NO_3_)3·9H_2_O competes with alkali metal halides, showing potential to induce halogenation of arenes. In this study, it was found that Fe(NO_3_)3·9H_2_O/KBr exhibits efficiency for the synthesis of p-bromoaromatic compounds at room temperature, while Fe(NO_3_)3·9H_2_O/KI is efficient for the synthesis of p-iodoaromatic compounds. Compared with the previous reports, a Fe(NO_3_)3·9H_2_O/alkali metal halide system could synthesize aryl halides at room temperature with high to excellent yields for substrates with an electron-donating group and low to moderate yields for substrates with an electron-withdrawing group. In addition, this protocol was readily scaled up to 15 mmol level without any loss of efficiency.^25^

Results and discussion

The initial step of the study was the optimization of reaction with Fe(NO_3_)3·9H_2_O(0.625 mmol)/KBr(0.625 mmol), using anisole (0.5 mmol) as a model substrate in various solvents for 2 h at room temperature (Table 1, entries 1–11). To our delight, para-bromination of anisole proceeded smoothly in CH_3_CN, giving the desired product in a high yield up to 99%. When the reaction was carried out in hexane, CH_2_Cl_2_, and EA, the brominated product was obtained in high yields up to 67%, 98% and 89%, respectively. Then, other types of Br sources such as NaBr, LiBr, CuBr_2_ or FeBr_3_ could also be applied in this reaction to give excellent yields (Table 1, entries 12–15). This indicated that Fe(NO_3_)3·9H_2_O combined with other bromine salts also successfully afforded 4-bromoanisole. In order to find the best method for the bromination of anisole, the reaction time and the ratio of Fe(NO_3_)3·9H_2_O/KBr were determined, which indicated that the optimum conditions are Fe(NO_3_)3·9H_2_O (0.625 mmol)/KBr(0.625 mmol) and a reaction time of 2 h (Table 1, entries 16–24). In addition, the reaction did not occur without Fe(NO_3_)3·9H_2_O (Table 1, entry 25). We also tested other types of Fe salts and nitrates, among which the desired product was offered by Cu(NO_3_)2 with 29% yield (Table 1, entries 26–31).

The obtained results for the reaction of para-bromination of anisole promoted our procedure to various anisole analogues (Table 2). Gratifyingly, the bromination of arenes containing electron-donating substituents such as alkoxy (Table 2, entries 1–5) and benzyloxy (Table 2, entry 6) proceeded smoothly to give the corresponding para-brominated products in good to excellent yields. Naphthyl substrates (Table 2, entries 7 and 8) were found to work well, giving the corresponding product in 86% and 97% yields. It is noteworthy that when 2-methoxynaphthalene reacted with multiple substrates under standard conditions but with the decreasing amount of Fe(NO_3_)3·9H_2_O to 0.25 mmol, the yield of desired product was increased to 87%. In addition, phenyl-, methyl-, and ethyl-substituted substrates also gave the corresponding products in high yields with monobromination at the para or ortho position with respect to the methoxyl substituent (Table 2, entries 9–13). Meanwhile, for weak electron-withdrawing substituted substrates, it offered the corresponding products in a relatively low yield, but when under adjusted conditions, the yield could be improved to a satisfactory value (Table 2, entries 14–19). However, for strong electron-withdrawing substituted substrates such as –CF_3_ and –CN, the reaction did not occur (Table 2, entries 20 and 21).

Meanwhile, the strong electron-donating groups on anisole should be reacted under optimized conditions, that is, some bromination products or nitrification products were obtained under standard conditions (Table 2, entries 22–26). For 1,2-dimethoxybenzene, the side product was a nitrification product (15%). While the amount of Fe(NO_3_)3·9H_2_O was decreased to 0.25 mmol, the yield of desired product was increased to 94%, and the yield of nitrification product was decreased to 5% (Table 2, entry 22). For 1,3-dimethoxybenzene, the desired product was obtained in 99% yield at the ratio of Fe(NO_3_)3·9H_2_O (0.25 mmol)/KBr(0.6 mmol) (Table 2, entry 23). For 1,4-dimethoxybenzene, the main product was a nitrification product with 83% yield (Table 2, entry 24). In addition, for 1,2,3-trimethoxybenzene, the highly electron-rich substrate afforded the desired product in 90% yield with a Fe(NO_3_)3·9H_2_O/KBr ratio of 0.375 mmol/1.5 mmol. It should note that 2,3-dimethoxybenzaldehyde could offer 65% yield at a reaction temperature of 60 °C. Moreover, acetyl aniline and phenyl ester were also found to be compatible with this catalytic protocol with high yields (Table 2, entries 29 and 30). We also tested toluene, aniline and phenol, but unfortunately, the reaction was sluggish.

Furthermore, it is notable that the present bromination could be scaled up to gram level: excellent yields of the corresponding products were obtained in one batch from 15 mmol of anisole and 3-methylanisole by using Fe(NO_3_)3·9H_2_O/KBr as an additive for 22 h (Scheme 1).

Scale-up of bromination by Fe(NO3)3·9H2O/KBr.

Inspired by the protocol of the bromination of anisole, the scope of the reaction was extended to iodination with Fe(NO_3_)3·9H_2_O/NaI (Table S1†). The results are provided in Table 3, which indicate that this protocol is suitable for the iodination of anisole analogues by Fe(NO_3_)3·9H_2_O/NaI with a ratio of 2 equiv./2 equiv. for 5 h at room temperature. In addition, the results were similar to those of the bromination process.

Moreover, possible mechanisms for the formation of the bromination are shown in Scheme 2. According to these results, that is, for 1,2-dimethoxybenzene, the side product was a nitro product (15%), and for 1,4-dimethoxybenzene, the main product was a nitrification product with 83% yield. Meanwhile, 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and 2,6-di-tert-butyl-4-methylphenol (BHT) are the generally accepted radical scavengers in organic chemistry. It was successfully found that the addition of TEMPO and BHT could influence the nitrification process very significantly. For example, a low yield of 2 was obtained when TEMPO (2%, 0.5 equiv.) or BHT (7%, 0.25 equiv.) was added, and the bromination process was affected to a small extent under the reaction condition (Table 4).

Possible mechanisms for bromination.

From these results, we propose a similar ionic pathway for our bromination process since our results are comparable with some of those works, 25a–c (Scheme 2). First, Fe(NO_3_)3·9H_2_O was reacted with Fe(OH)3 and H^+^ (eqn (1)), and then NO_3_^−^ was converted into ^+^NO_2_ (eqn (2)). The bromide ion (Br^−^) from KBr would be reacted with ^−^NO_3_ and H^+^ to generate intermediate Br_2_ (eqn (3)). Then, unstable nitryl bromide (BrNO_2_) was formed and depending on the substrate nature, it could act as electrophilic and radical species (eqn (4) and (5)). It was presumed that the bromination process involves typical electrophilic bromination to a large extent.

Conclusions

In conclusion, we have developed a simple, efficient and environmentally friendly methodology for the halogenation of anisole analogues using Fe(NO_3_)3·9H_2_O/KBr or NaI at room temperature. In this method, substrates with an electron-donating group afforded the corresponding product in good to excellent yields, while those with an electron-withdrawing group gave low to moderate yields. More importantly, this protocol is also applicable to gram-scale synthesis. It is hoped that this methodology will be very much useful in organic synthesis.

Data availability

The authors confirm that the data supporting the findings of this study are available within the article and its ESI.†

Author contributions

Conceptualization: Huanjun Xu and Yiying Li; methodology: Caicui Li, Yao Cheng and Fudan Pang; formal analysis: Xinmei Wang and Xiaodan Wang; investigation: Caicui Li, Xiushuo Yan, Zhengtao Huang and Yao Cheng; resources: Yiying Li, Huanjun Xu and Jinhui Wang; writing – original draft preparation: Xiaodan Wang and Huanjun Xu; writing – review and editing: Huanjun Xu and Jinhui Wang; supervision: Yiying Li and Huanjun Xu; project administration: Huanjun Xu; and funding acquisition: Yiying Li, Huanjun Xu and Jinhui Wang. All the authors have read and agreed to the published version of the manuscript.

Conflicts of interest

There are no conflicts to declare.

Supplementary Material

RA-015-D5RA00837A-s001