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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731927Generated: October 31, 2026

N-bromobutanimide → Ethyl 2-(bromomethyl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/731927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-methylbiphenyl-4-carboxylateHCID 23112239—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-(bromomethyl)biphenyl-4-carboxylateHCID 23112214758.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

In 130 ml of carbon tetrachloride was dissolved 10 g of ethyl 2-methylbiphenyl-4-carboxylate, the whole was heated to 90° C. and then 1.0 g of NBS and 136 mg of 2,2′-azobisisobutyronitrile were added thereto. After the reaction solution was heated under reflux, 6.78 g of NBS was added thereto and the whole was heated under reflux for 1 hour and a half. After the reaction solution was cooled to room temperature, precipitate was removed by filtration, water was added to the filtrate, and the organic layer was extracted with carbon tetrachloride. After the resulting organic layer was dried over anhydrous magnesium sulfate, the solvent was removed by evaporation to obtain 13.6 g of ethyl 2-(bromomethyl)biphenyl-4-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585878B2
Source datasetuspto-grants-2009_09
ORD IDord-145528f9e8a64739a3104fd160de4055
Source noteuspto-grants-2009_09