HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253016Generated: October 31, 2026
Gamma-Aminobutyric Acid → 4-[(2-Methylacryloyl)amino]butanoic acid
https://huagongshe.com/reaction/1253016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-[(2-Methylacryloyl)amino]butanoic acid | HCID 18798151 | 89.8% |
Reaction Steps
In a solution of 38 g of sodium hydroxide, 200 ml of water, and 2 ml of nitrobenzene was dissolved 100 g of γ-aminobutyric acid while stirring, followed by cooling to 0° C. To the aqueous solution were added simultaneously 107.5 g of methacryl chloride and an aqueous solution of 45 g of sodium hydroxide in 100 ml of water. After completion of the reaction, 400 ml of acetonitrile was added thereto. After the reaction mixture was made acidic with 80 ml of concentrated hydrochloric acid, the mixture was extracted with acetonitrile. The resulting acetonitrile extract was concentrated to obtain 149 g of oily N-methacryloyl-γ-aminobutyric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04746602 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-0e86536023684d4a9eadb17bb295139b |
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| Source note | uspto-grants-1988_05 |
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