Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916749Generated: October 26, 2026

Hydrogen Bromide → [1-(Bromomethyl)cyclopropyl]methyl acetate

https://huagongshe.com/reaction/916749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,1-Bis(hydroxymethyl)cyclopropaneHCID 4101437—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product[1-(Bromomethyl)cyclopropyl]methyl acetateHCID 5896161381.4%

Reaction Steps

A 50 mL 3-neck round bottle flask was equipped with condenser, an addition funnel and a thermometer. Charge 2 g of 1,1-cyclopropyldimethanol, 5 g of acetic anhydride, 2 mL of methylene chloride and 0.77 g of pyridine to the flask. The reaction mixture was heated to about 90˜95° C. and kept continuous stirring about 1 hour. When the reaction was completed, the mixture was cooled and the 14.4 g of 33% HBr in glacial acetic acid was added while maintain below 20° C. After the addition, the reaction mixture was stirred about 6 hours and then 2 mL of methylene chloride and 10 mL of water was added into the flask. The layers were separated and the aqueous layer was extracted twice with 4 mL of methylene chloride. Combined the organic layers and washed twice with 6 mL of water and then neutralized to pH=8 with sodium carbonate solution. The organic layers were concentrated to obtain 3.3 g of crude [1-(bromomethyl)cyclopropyl]methyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271268B1
Source datasetuspto-grants-2007_09
ORD IDord-7882bd122eb841a5beebd2f886fcadee
Source noteuspto-grants-2007_09