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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379870Generated: October 27, 2026

Bromine → 3'-Bromo-4'-methyl-1,1'-biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1379870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2-Cyano-4'-methylbiphenylHCID 145512—
CatalystSilver trifluoroacetateHCID 76299—
SolventDichloromethaneHCID 6344—
Product3'-Bromo-4'-methyl-1,1'-biphenyl-2-carbonitrileHCID 2184033841%

Reaction Steps

A solution of 5.2 g (27 mmol) of 4'-methyl-1,1'-biphenyl-2-nitrile (Step B) in 60 mL of methylene chloride at 0° C. was treated with 6.7 g of silver trifluoroacetate (30 mmol). When all the silver trifluoroacetate was dissolved, 1.6 mL of bromine was added dropwise (4.95 g, 31 mmol) with vigorous stirring. After two hours, the reaction mixture was filtered and the solid washed with methylene chloride. The combined organic layers were washed once with dilute (<1 N) aqueous sodium hydroxide and once with brine. The organic layer was removed, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue was purified by preparative high pressure liquid chromatography on silica, eluting with 10% etherexane to give 3 g (41%) of product. 1H NMR (200 MHz, CDCl3): δ 2.46 (s, 3H), 7.2-7.8 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05672596
Source datasetuspto-grants-1997_09
ORD IDord-4185e0fe494f49f1bad06eb976f70b2d
Source noteuspto-grants-1997_09