HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861598Generated: November 2, 2026
Gamma-Aminobutyric Acid → 4-(((Benzyloxy)carbonyl)amino)butanoic acid
https://huagongshe.com/reaction/1861598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(((Benzyloxy)carbonyl)amino)butanoic acid | HCID 21184 | — |
Reaction Steps
A solution of benzylchloroformate (9.4 g, 5.5 mmol) in acetone (15 ml) was added dropwise to a mixture of 4-aminobutanoic acid (5.2 g, 5 mmol), sodium bicarbonate (8.6 g, 10 mmol), water (25 ml) and acetone (25 ml) causing vigorous effervescence. The solution was allowed to stir overnight. The acetone was removed using a rotary evaporator to leave an aqueous phase which was washed with ether (2×25 ml). The resulting aqueous layer was acidified to pH2 with dilute hydrochloric acid and then extracted with dichloromethane (3×50 ml). The dichloromethane extracts were combined, dried over magnesium sulphate and volatile components removed under reduced pressure to leave 4-[(benzyloxycarbonyl)amino]butanoic acid as a white solid in a good state of purity. This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06534488B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-b4a092e576844b9e8acf7be42d2fcc8c |
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| Source note | uspto-grants-2003_03 |
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