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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356567Generated: October 26, 2026

Acetic Acid → (3S)-3-acetyloxy-4-bromobutanoic acid

https://huagongshe.com/reaction/1356567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
Reactant3-Hydroxybutyrolactone, (3S)-HCID 7269389—
SolventDichloromethaneHCID 6344—
Product(3S)-3-acetyloxy-4-bromobutanoic acidHCID 273388095%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a 2 l of three-necked flask equipped with reflux condenser, thermometer and mechanical stirrer were charged (S)-3-hydroxy-γ-butyrolactone (102 g) and 30% of hydrobromic acid in acetic acid (675 g, 2.5 eq.). The mixture was stirred at 40° C. for 3 hours. After cooling the reaction mixture, methylene chloride (1000 ml) was added to it. The reaction mixture was washed with aqueous solution of sodium acetate. The organic layer was separated, dried over magnesium sulfate, and concentrated to afford (S)-3-acetoxy-4-bromobutyric acid (213 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586616B1
Source datasetuspto-grants-2003_07
ORD IDord-811ace35f479451696a4894ed030bdba
Source noteuspto-grants-2003_07