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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980504Generated: October 30, 2026

p-Bromochlorobenzene → HCID 12501054, compound

https://huagongshe.com/reaction/1980504

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantHCID 57370169HCID 57370169—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventLithium ChlorideHCID 433294—
ProductHCID 12501054HCID 1250105412%

Reaction Steps

A solution of 14.4 g (0.075 mol) of 4-bromochlorobenzene and 9.5 ml (12.3 g, 0.075 mol) of chloromethyl(dichloro)methylsilane in 150 ml of tetrahydrofuran was cooled to -60° under nitrogen and stirred while 94 ml (0.15 mol) of 1.6 molar n-butyllithium in hexane was added dropwise at a rate that held the mixture between -65° and -55°. The resulting slurry was allowed to warm to room temperature, giving a solution that was diluted with hexanes until no more lithium chloride precipitated. Filtration, evaporation of the filtrate, dissolution of the residue in hexanes, refiltration, and evaporation left 19.8 g of a pale orange liquid. Distillation gave first 1.8 g (12%) of chloromethyl(dibutyl)methylsilane, bp 45° C. (0.05 mm), followed by 6.8 g (35%) of the title compound as a colorless liquid: bp 90° C. (0.05 mm); nD21 1.5246; ir (neat) 2925, 1580, 1380, 1260, 1090, 1015, 820, 740 cm-1 ; nmr (CDCl3) 0.4 (3H, s), 0.6-1.5 (9H, m), 2.9 (2H, s), 7.0-7.4 (4H, q).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510136
Source datasetuspto-grants-1985_04
ORD IDord-c0d1f7c977d54dd5aaf8e935780b717c
Source noteuspto-grants-1985_04