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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594658Generated: November 4, 2026

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

https://huagongshe.com/reaction/1594658

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 numberUS06284768B1
Source datasetuspto-grants-2001_09
ORD IDord-86bafae9a2f2404b8299666ac0eb2f7b
Source noteuspto-grants-2001_09