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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005395Generated: October 26, 2026

N-bromobutanimide → Ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate

https://huagongshe.com/reaction/1005395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 1-methyl-1-(4-methylphenyl)ethanesulfonateHCID 21706484—
CatalystBenzoyl chlorideHCID 7412—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonateHCID 21706518105.4%

Reaction Steps

To a solution of ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate (0.458 g, 1.89 mmol) in carbon tetrachloride (8 mL) was added N-bromosuccinimide (0.370 g, 2.08 mmol) and benzoyl chloride (0.009 g). The mixture was heated under reflux for 1.5 hours, cooled to rt, and filtered. The filtrate was washed with aqueous sodium bicarbonate and brine, dried, filtered and evaporated to give crude ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate (0.64 g, 100%) which was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054470
Source datasetuspto-grants-2000_04
ORD IDord-e2447f1540014d6c84d0a72d1913ca49
Source noteuspto-grants-2000_04