# Synthesis of Polyimides, Polyamides, and Poly(Amide-Imides) in the “Green” Solvent N-Butyl-2-Pyrrolidone (TamiSolve NxG): Features, Optimization, and Versatility

**Authors:** Olesya N. Zabegaeva, Alexander V. Chuchalov, Dmitriy A. Khanin, Denis O. Ponkratov, Dmitriy A. Sapozhnikov

PMC · DOI: 10.3390/ijms27031252 · International Journal of Molecular Sciences · 2026-01-27

## TL;DR

This paper explores replacing toxic solvents with a green alternative, N-butyl-2-pyrrolidone, for synthesizing high-performance polymers like polyimides and polyamides.

## Contribution

The study introduces N-butyl-2-pyrrolidone as a sustainable solvent for polymer synthesis, achieving high molecular weights and tunable properties.

## Key findings

- N-butyl-2-pyrrolidone successfully replaces toxic solvents in synthesizing polyimides, polyamides, and poly(amide-imides).
- Optimized conditions yielded high-molecular-weight polymers (Mn = 37–346 kDa; Mw = 133–537 kDa).
- The solvent enables synthesis of polymers with diverse chemical structures and tunable molecular weights.

## Abstract

Owing to their outstanding thermal and mechanical properties, polyimides (PIs), polyamides (PAs), and poly(amide-imides) (PAIs) are essential for developing and manufacturing modern high-tech products, including electroactive ones. Despite their large-scale production for diverse applications, the synthesis of these polymers traditionally relies on highly toxic solvents such as N,N-dimethylacetamide, N,N-dimethylformamide, N-methyl-2-pyrrolidone (NMP), and m-cresol. This work investigates the possibility of replacing these hazardous solvents with a more sustainable and “green” alternative, N-butyl-2-pyrrolidone (NBP). We have thoroughly studied and analyzed the synthesis of various PIs, PAs, and PAIs via one- and two-step polycondensation of tetracarboxylic acid dianhydrides with diamines, low-temperature polycondensation of terephthaloyl chloride with diamines, and low-temperature polycondensation of tetracarboxylic acid dianhydrides and terephthaloyl chloride with diamines, respectively. Our results demonstrate that substituting NBP for NMP presents distinct characteristics and outcomes for each process. By optimizing the reaction conditions, we were able to obtain high-molecular-weight products (Mn = 37–346 kDa; Mw = 133–537 kDa) for all polymer classes studied. Thus, this work establishes NBP as a suitable and promising solvent for synthesizing PIs, PAs, and PAIs with diverse chemical structures and tunable molecular weight characteristics.

## Linked entities

- **Chemicals:** N-butyl-2-pyrrolidone (PubChem CID 18984), N,N-dimethylacetamide (PubChem CID 14470), N,N-dimethylformamide (PubChem CID 6228), N-methyl-2-pyrrolidone (PubChem CID 13387), m-cresol (PubChem CID 342), terephthaloyl chloride (PubChem CID 7488)

## Full-text entities

- **Chemicals:** m-cresol (MESH:C042041), N,N-dimethylformamide (MESH:D004126), N-Butyl-2-Pyrrolidone (-), N,N-dimethylacetamide (MESH:C013959), terephthaloyl chloride (MESH:C059743), diamines (MESH:D003959), N-methyl-2-pyrrolidone (MESH:C038678), PAs (MESH:D009757), polymer (MESH:D011108)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12898531/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12898531/full.md

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Source: https://tomesphere.com/paper/PMC12898531