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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372448Generated: October 30, 2026

Azobisisobutyronitrile → Methyl 4'-(bromomethyl)biphenyl-2-carboxylate

https://huagongshe.com/reaction/2372448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant(1,1'-Biphenyl)-2-carboxylic acid, 4'-methyl-, methyl esterHCID 1393873—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4'-(bromomethyl)biphenyl-2-carboxylateHCID 1101218178%

Reaction Steps

A 47.46 g (210 mmol) sample of methyl 2-(p-tolyl)benzoate (Chemo Dynamics Inc.) was dissolved in 3 L of carbon tetrachloride and treated with 37.33 g (209 mmol) of N-bromosuccinimide (NBS) and 1.17 g (7.13 mmol) of azobisisobutyronitrile (AIBN) at reflux under nitrogen for 24 hours. The reaction mixture was treated again with 1.0 g (6.1 mmol) of AIBN and stirred at reflux for an additional 24 hours. The reaction was filtered and the solvent removed in in vacuo. Purification by silica gel chromatography (Waters Prep-500A) using ethyl acetate/hexane (5:95) as eluent provided 50.0 g (78%) of a colorless solid: mp 48°-51° C.; NMR (CDCl3) δ 3.64 (s, 3H), 4.54 (s, 2H), 7.23-7.63 (m, 7H), 7.81-7.89 (m, 1H). NMR indicated that this material was only 91% pure; it contained 9% of the corresponding dibromocompound (δ 6.70 ); however, no further attempts at purification were made and this mixture was used in all subsequent alkylation reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05098920
Source datasetuspto-grants-1992_03
ORD IDord-85a442a6c27048508e57e97a15caefa1
Source noteuspto-grants-1992_03