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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539848Generated: October 31, 2026

Benzoyl Peroxide → Biphenyl-4-yl-bromo-acetic acid methyl ester

https://huagongshe.com/reaction/539848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Biphenylylacetic acid methyl esterHCID 3080863—
ReactantAcetonitrile--water (1/1)HCID 18373917—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductBiphenyl-4-yl-bromo-acetic acid methyl esterHCID 1182288093%

Reaction Steps

To a stirred solution of biphenyl-4-yl-acetic acid methyl ester (5 g., 22.1 mmol) in carbon tetrachloride (from Acros, 16772) (25 mL) was added N-bromosuccinimide (from Aldrich, 18350) (3.9 g., 22.1 mmol) and benzoyl peroxide (from Acros, 21178) (0.54 g, 2.2 mmol) and the reaction was heated to reflux for 48 hours. The reaction mixture was cooled to room temperature, filtered and the filtrate concentrated in vacuo to afford Cpd. 2 as a crude yellow oil (6.24 g., 93% yield). 1HNMR (CDCl3) δH, 3.81, 3H (s, CH3), 5.41, 1H (s, Br—CH), 7.33-7.39, 2H (m, Ar—H), 7.41-7.46, 3H (m, Ar—H), 7.54-7.63, 4H (m, Ar—H); LCMS analysis (solvent MeCN/H2O/0.1% HCO2H, 5-95% gradient/H2O 2.5 min, 95% 4 min., Phenomenex C18 reverse phase, flow rate 1 mL/min.) HPLC retention time 4.39 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871772B2
Source datasetuspto-grants-2014_10
ORD IDord-2b653551695c4e319803072aed7ec319
Source noteuspto-grants-2014_10