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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379686Generated: October 30, 2026

p-Bromochlorobenzene → HCID 12319462, compound

https://huagongshe.com/reaction/2379686

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductHCID 12319462HCID 1231946299%

Reaction Steps

A solution of 23.0 g (120 mmole) of 4-bromochlorobenzene in 150 ml of dry tetrahydrofura: was cooled to -78° C. under nitrogen and 78 ml (120 mmole) of 1.55M n-butyllithium in hexane was added dropwise at a rate to maintain temperature below -60° C. After stirring an additional 15 minutes, 14.0 ml (120 mmole) of 2-bromo-benzaldehyde was added and the reaction was stirred for 15 minutes. The reaction was quenched at -78° C. with saturated aqueous ammonium chloride and allowed to warm to room temperature. The reaction solution was diluted with 300 ml of diethyl ether and washed with three 75 ml portions of 1.0M sodium bisulfite, followed by 50 ml of 1.0M sodium hydroxide, 100 ml of water, and 50 ml of saturated sodium chloride. After drying over magnesium sulfate, the solvent was removed to give 35.3 g (99%) of crude 2-bromo-α -(4-chlorophenyl)benzyl alcohol as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364843
Source datasetuspto-grants-1994_11
ORD IDord-754a148e2ecc45f5a9118bcffc5f6755
Source noteuspto-grants-1994_11