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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710001Generated: October 31, 2026

N-bromobutanimide → 2-Hydroxy-3-bromo-4-chloro-5-(1,1-dimethylethyl)benzaldehyde

https://huagongshe.com/reaction/1710001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Hydroxy-4-chloro-5-(1,1-dimethylethyl)benzaldehydeHCID 23035427—
SolventDichloromethaneHCID 6344—
Product2-Hydroxy-3-bromo-4-chloro-5-(1,1-dimethylethyl)benzaldehydeHCID 2303541581.3%

Reaction Steps

A solution of 1.84 g (8.65 mmol) of 2-hydroxy-4-chloro-5-(1,1-dimethylethyl)benzaldehyde and 1.85 g (10.4 mmol) of N-bromosuccinimide in 30 ml of methylene chloride was stirred overnight at ambient temperature. The solvent was evaporated and the residue was partitioned between water and hexane. The organic phase was dried and evaporated. The residue was chromatographed on 150 g of silica gel using a gradient from 1:99 to 5:95 (v/v) of ether:hexane as eluent. There was obtained 2.05 g (7.03 mmol, 81%) of 2-hydroxy-3-bromo-4-chloro-5-(1,1-dimethylethyl)benzaldehyde after crystallization from hexane; mp 92°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952583
Source datasetuspto-grants-1990_08
ORD IDord-38bcc792b31a469d9451ae6b9a8e20c8
Source noteuspto-grants-1990_08