HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413014Generated: October 30, 2026
Gamma-Aminobutyric Acid → 4-[(2-Methylacryloyl)amino]butanoic acid
https://huagongshe.com/reaction/2413014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[(2-Methylacryloyl)amino]butanoic acid | HCID 18798151 | 93% |
Reaction Steps
In a mixture composed of 80 g (2.0 mols) of sodium hydroxide, 400 ml of water and 4 ml of nitrobenzene was dissolved with stirring 214 g (2.0 mols) of γ-aminobutyric acid and the resulting solution was cooled to 0° C. To the aqueous solution, there were simultaneously. added dropwise 230 g (2.2 mols) of methacrylic chloride and an aqueous solution containing 96 g (2.4 mols) of sodium hydroxide dissolved in 200 ml of water. After the completion of the reaction, 800 ml of acetonitrile was added to the reaction solution and the mixture was then acidified by adding 160 ml of concentrated hydrochloric acid and extracted with acetonitrile. The acetonitrile solution was concentrated to obtain 318.4 g of N-methacryloyl-γ-aminobutyric acid as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04495272 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-9fdb71c7df4b49dd98ffa1565be79658 |
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| Source note | uspto-grants-1985_01 |
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