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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247767Generated: October 26, 2026

Dichloromethane → 2-Bromo-1-(oxolan-2-yl)ethan-1-one

https://huagongshe.com/reaction/1247767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-(Oxolan-2-yl)ethan-1-oneHCID 18965—
ReactantN-bromobutanimideHCID 67184—
ReactantTrimethylsilane triflateHCID 131726018—
SolventTriethylamineHCID 8471—
Product2-Bromo-1-(oxolan-2-yl)ethan-1-oneHCID 21908965—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a 20-liter glass vessel was added methylene chloride (10.0 liters) followed by acetyltetrahydrofuran (838.0 g, 7.34 moles). The solution was then cooled back to −10° C. and triethylamine was added (854.0 g, 8.44 moles). The vessel was purged with nitrogen and trimethylsilane triflate (1713.0 g, 7.71 moles) was added dropwise at a maximum temperature of −8° C. Addition was typically complete in 45 minutes. After 15 minutes stirring, a sample was removed for TLC and GC analysis, which showed that the reaction was completed. N-bromosuccinimide (1340 g. 7.53 moles) was added to the solution at a maximum temperature of −5° C. over a period of approximately 45 minutes in six portions. After a 30 minute stirring, the solution was sampled for GC and TLC analysis, which showed that the reaction was completed. The solution was then transferred to a 50-liter separating vessel, and 5% sodium bicarbonate (5 liters) was added with caution. The solution was stirred and separated. The upper aqueous phase was discarded, and the methylene chloride phase was washed with water, dried over sodium sulphate, filtered and stored in a freezer before use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129350B2
Source datasetuspto-grants-2006_10
ORD IDord-bcc7dca928fb4ee3b89c645a86fd1cb6
Source noteuspto-grants-2006_10