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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980507Generated: November 1, 2026

p-Bromochlorobenzene → HCID 131714090, compound

https://huagongshe.com/reaction/1980507

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
Reactant1-Bromo-2-chlorobenzeneHCID 12754—
ReactantHCID 57370169HCID 57370169—
ReactantHCID 178418244HCID 178418244—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 131714090HCID 13171409095%

Reaction Steps

A solution of 6.3 ml (8.2 g, 0.05 mol) of chloromethyl(dichloro)methylsilane and 8.1 g (0.05 mol) of 2-bromochlorobenzene in 75 ml of dry tetrahydrofuran was chilled to -60° under N2 and stirred while 31 ml (0.05 mol) of 1.6 molar n-butyllithiumhexane solution was added at a rate that held the mixture below -55°. With continued cooling and stirring, 8.1 g (0.05 mol) of 4-bromochlorobenzene was added as a solid, followed by another 31 ml portion of the 1.6 molar n-butyllithium solution at a rate that held the mixture below -55° C. The resulting thin slurry was allowed to warm to room temperature, treated cautiously with 10 ml of ethyl acetate, and worked up as in Example 8 to give 15.0 g of a clear yellow oil. Distillation provided 5.9 g (37%) of the title compound: bp 150°-165° (0.7 mm); nD20 1.5916; ir (neat) 3060, 3020, 2960, 2920, 2870, 1580, 1560, 1490, 1420, 1380, 1255, 1125, 1115, 1085, 1035, 1015, 805, 750 cm-1 ; nmr (CDCl3) 0.8 (3H, s), 3.3 (2H, s), 7.2-7.7 (8H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510136
Source datasetuspto-grants-1985_04
ORD IDord-0c7ade39782f4c489410a7f9b31f2606
Source noteuspto-grants-1985_04