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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857828Generated: November 2, 2026

Acetic Anhydride → Butyl 2-methylene-3-acetoxy-4,4,4-trichlorobutyrate

https://huagongshe.com/reaction/1857828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
ReactantHCID 18362110HCID 18362110—
CatalystSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
ProductButyl 2-methylene-3-acetoxy-4,4,4-trichlorobutyrateHCID 1122084491.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

To 1173.0 g of butyl 2-methylene-3-hydroxy-4,4,4-trichlorobutyrate (91% pure) charged in a 2-liter, 3-neck round bottom flask equipped with a mechanical stirrer, thermometer, and a condenser were added 520.0 g of acetic anhydride and 7.0 g of sodium acetate. The reaction mixture was heated at 120° C. for three hours. Unreacted acetic to anhydride and formed acetic acid were stripped off under vacuum at <80° C./0.6 mm Hg. After cooling to room temperature, the solid sodium acetate that had settled to the bottom of the flask was separated. 1236.1 g of acetylated product was obtained, 91.3% purity (GC analysis), 91.4% yield. The product structure was confirmed by NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147251
Source datasetuspto-grants-2000_11
ORD IDord-71a1bab6b31c4f29b72a908131e768c5
Source noteuspto-grants-2000_11