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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845217Generated: October 30, 2026

p-Bromochlorobenzene → HCID 53634461, compound

https://huagongshe.com/reaction/845217

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 53634461HCID 53634461100.8%

Reaction Steps

A solution of 4-bromochlorobenzene (20.0 g, 104 mmol) in 125 mL of dry tetrahydrofuran under nitrogen was cooled to -78° and 70 mL of 1.5M n-butyllithium in hexane was added dropwise over 20 minutes. After stirring another 10 minutes, 12.5 mL (104 mmol) of 3-bromobenzaldehyde was added dropwise and the reaction was stirred for another 10 minutes at -78°. Saturated aqueous ammonium chloride (100 mL) was added and the reaction was warmed to room temperature and extracted with 300 mL of ether. The ethereal layer was extracted with three 75 mL portions of 1M sodium bisulfite, 75 mL of 1M sodium hydroxide, 75 mL of water, and 75 mL of brine. The ether layer was dried over magnesium sulfate and the solvent removed to give 31.2 g of 3-bromo-4'-chlorobenzhydryl alcohol as a pale yellow solid. A portion was recrystallized from hexanes containing 5% ether to give white needles, m.p. 67°-68°. Calc. for C13H10Br C10: C, 52.47; H, 3.39; Br, 26.85; Cl, 11.91. Found: C, 52.25; H, 3.25; Br, 26.72; Cl, 12.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04757074
Source datasetuspto-grants-1988_07
ORD IDord-4b7a89302dc948ad92ef17e154c04e28
Source noteuspto-grants-1988_07