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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601452Generated: November 1, 2026

N-bromobutanimide → 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one

https://huagongshe.com/reaction/1601452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4,5-Dimethyl-1,3-dioxol-2-oneHCID 142210—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141112.3%

Reaction Steps

Combine 4,5-dimethyl-1,3-dioxol-2-one (3.42 g, 30 mmol), N-bromosuccinimide (5.34 g, 30 mmol) and AIBN (500 mg, 3 mmol) in anhydrous carbon tetrachloride (100 mL). Heat at reflux. After 2 hours, cool and filter. Concentrate the filtrate to give 4-bromomethyl-5-methyl-1,3-dioxol-2-one (6.5 g, crude) as an oil, which can be used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977139
Source datasetuspto-grants-1999_11
ORD IDord-4a4501c9981543c0ae844cfdfd3cfbf1
Source noteuspto-grants-1999_11