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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230234Generated: October 25, 2026

Benzoyl Peroxide → Methyl 5-bromo-2-(bromomethyl)benzoate

https://huagongshe.com/reaction/230234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 5-bromo-2-methylbenzoateHCID 316201—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 5-bromo-2-(bromomethyl)benzoateHCID 12929136—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-Bromo-2-methyl-benzoic acid methyl ester (1.31 g, 5.72 mmol) was dissolved in carbon tetrachloride (40 mL). Benzoyl peroxide (10-20 mg) and NBS (1.01 g, 5.72 mmol) were added and the reaction mixture was heated to reflux at 100° C. The reaction course was followed by HPLC and determined to be complete after 1.25 hours. Silica gel was added and the solvent was removed under reduced pressure. The material was purified on silica gel using 5% ethyl acetate in hexanes as the eluent and was determined to be 85% pure by NMR (contained 10% starting material and 5% 5-bromo-2,2-dibromomethyl-benzoic acid methyl ester) and then used without further purification. 1H NMR (300.132 MHz, CDCl3) δ 8.10 (d, J=2.2 Hz, 1H), 7.62 (dd, J=8.3, 2.1 Hz, 1H), 7.34 (d, J=8.5 Hz, 1H), 4.90 (s, 2H), 4.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566727B2
Source datasetuspto-grants-2009_07
ORD IDord-d587078cc49647c0b401dcc940a3b844
Source noteuspto-grants-2009_07