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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893615Generated: October 30, 2026

N-bromobutanimide → Methyl 4'-(bromomethyl)biphenyl-2-carboxylate

https://huagongshe.com/reaction/893615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(1,1'-Biphenyl)-2-carboxylic acid, 4'-methyl-, methyl esterHCID 1393873—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4'-(bromomethyl)biphenyl-2-carboxylateHCID 1101218186.9%

Reaction Steps

N-Bromosuccinimide (8.1 g) and azo(bisisobutyronitrile) (130 mg) were added to a solution of compound (B1) (9.3 g) in carbon tetrachloride (300 ml). The mixture was heated under reflux for 4 hours and then cooled to ambient temperature. Insoluble material was removed by filtration and the filtrate concentrated. The residue was purified by flash chromatography, eluting with ethyl acetate/hexane (1:9 v/v) to give methyl 4'-(bromomethyl)biphenyl-2-carboxylate (C1) as a solid (10.9 g), m.p. 48°-50° C.; NMR: 3.65(s,3H), 4.55(s,2H), 7.25-7.60 (complex m,7H), 7.85(d,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126344
Source datasetuspto-grants-1992_06
ORD IDord-61973961178c4d1781b1387138669af8
Source noteuspto-grants-1992_06