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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298141Generated: October 30, 2026

Azobisisobutyronitrile → (3-Bromomethyl-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/2298141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-(m-tolyl)acetateHCID 5135288—
SolventCarbon TetrachlorideHCID 5943—
Product(3-Bromomethyl-phenyl)-acetic acid methyl esterHCID 10014651—

Reaction Steps

A solution of m-toly-acetic Acid methyl ester (11.41 g, 69.49 mmol), N-bromosuccinimide (12.59 g, 70.73 mmol), AIBN (100 mg) in CCl4 (200 mL) was heated at reflux for 16 h. The reaction was cooled to room temperature and aqueuos NaHCO3 (satd) was added. The aqueous solution was extracted with CH2Cl2 (2×) and the organic solution was dried (MgSO4), filtered, and concentrated. Purification by flash chromatography (hexanes to 9:1 hexanes:EtOAc) provided the title compound as a clear and colorless liquid (11.99 g). 1H NMR (CDCl3 400 MHz) δ 7.27 (m, 4H), 4.47 (s, 2H), 3.69 (s, 3H), 3.62 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-8669669b32d74fdeaa3b6e52be818979
Source noteuspto-grants-2002_12