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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088911Generated: November 2, 2026

Acetyl chloride → (2S,3R)-2-bromo-3-acetoxy-butyryl chloride

https://huagongshe.com/reaction/1088911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantOxalyl chlorideHCID 65578—
Reactant(2S,3R)-2-bromo-3-hydroxybutanoic acidHCID 10921164—
Product(2S,3R)-2-bromo-3-acetoxy-butyryl chlorideHCID 10955782—

Reaction Conditions

Temperature5 °C

Reaction Steps

Acetyl chloride (6.82 g, 86.88 mmole) was added dropwise to (2S, 3R)-2-bromo-3-hydroxybutyric acid (neat) with stirring. The reaction mixture was cooled in a bath at 5° C. as exotherm began. After completion of addition, the cooling bath was removed. After 45 minutes the mixture was heated at 45°-50° C. for 1.5 hours. Heating was discontinued and 10 mL toluene was added. The mixture was cooled in an ice bath and oxalyl chloride (11.4 80 g, 90.44 mmole) was added dropwise. After completion of addition, the mixture was allowed to warm to room temperature then heated at reflux for 30 minutes. Toluene and excess of reagents were removed by fractional distillation. The residue was subjected to bulb-to-bulb distillation at 80°-90° C. under high vacuum (1 mm/Hg) to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963670
Source datasetuspto-grants-1990_10
ORD IDord-b0d6c0974f804fd1b098638f8275dbb4
Source noteuspto-grants-1990_10