Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077119Generated: November 4, 2026

N-bromobutanimide → 2-Bromomethyl-3-phenoxy-benzoic acid ethyl ester

https://huagongshe.com/reaction/2077119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-3-phenoxy-benzoic acid ethyl esterHCID 67110135—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromomethyl-3-phenoxy-benzoic acid ethyl esterHCID 67110121105.6%

Reaction Steps

A mixture of 2-methyl-3-phenoxy-benzoic acid ethyl ester (5.23 g, 0.02 mol), N-bromosuccinimide (3.82 g, 0.02 mol) and benzoyl peroxide (247.5 mg, 1.1 mmol) in carbon tetrachloride (80 mL) was refluxed for 4 h before it was cooled to room temperature and filtered. The filtrate was washed with water, saturated aqueous sodium bicarbonate solution, and brine before it was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a yellow oil (7.08 g): 1H NMR (CDCl3, 200 MHz): δ=7.66 (m, 1H), 7.24 (m, 3H), 7.03 (m, 1H), 6.98 (m, 3H), 5.09 (s, 3H), 4.42 (q, J=7.2 Hz, 2H), 1.44 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928120B2
Source datasetuspto-grants-2011_04
ORD IDord-e8d91435b12c461f83fc28f1fcbbfb04
Source noteuspto-grants-2011_04