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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413302Generated: October 31, 2026

4-Bromobiphenyl → HCID 13392401, compound

https://huagongshe.com/reaction/2413302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobiphenylHCID 7101—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantMagnesiumHCID 5462224—
ReactantHCID 57370169HCID 57370169—
SolventIsopropanolHCID 3776—
ProductHCID 13392401HCID 1339240196%

Reaction Steps

A solution of 73.3 g (0.315 mol) of 4-bromobiphenyl in 300 ml of tetrahydrofuran was added dropwise to a stirred suspension of 7.64 g (0.315 mol) of magnesium in 100 ml of tetrahydrofuran at a rate that maintained gentle reflux. The resulting clear solution was stirred at room temperature for 1 hour and then cooled in ice, and a solution of 40 ml (0.315 mol) of chloromethyl(dichloro)methylsilane in 100 ml of tetrahydrofuran was added rapidly. The resulting solution was stirred at room temperature for 20 hours, treated with 50 ml of isopropanol, and cooled in ice again. A solution of 48 ml (0.344 mol) of triethylamine in tetrahydrofuran was then added at a rate that held the mixture below 25°. Stirring at room temperature for 90 minutes gave a slurry. Filtration, evaporation of the filtrate, trituration with hexanes, and a second filtration removed residual amine hydrochloride. Evaporation of the hexanes solution gave 92 g (96%) of the title compound as a pale yellow oil that solidified on standing; m.p. 35°-38°; nmr (CDCl3) 0.5 (3H, s), 1.2 (6H, d), 3.0 (2H, s), 4.2 (1H, septet), 7.3-7.8 (9H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496551
Source datasetuspto-grants-1985_01
ORD IDord-1769e83f2ebd43b283c1253817bfff5d
Source noteuspto-grants-1985_01