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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875096Generated: November 3, 2026

N-bromobutanimide → 3-{[3-(Bromomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrile

https://huagongshe.com/reaction/1875096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Chloro-5-[(2,6-difluoro-3-methylphenyl)oxy]benzonitrileHCID 68486606—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product3-{[3-(Bromomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrileHCID 6848536856%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 3-chloro-5-[(2,6-difluoro-3-methylphenyl)oxy]benzonitrile (4.05 g, 14.48 mmol) and NBS (3.09 g, 17.38 mmol) in carbon tetrachloride (500 mL) was degassed and heated to 90° C. under a nitrogen atmosphere. After ca. 5 min, AIBN (0.119 g, 0.724 mmol) was added and the solution was heated for 6 h. The solution was cooled to 0° C. then filtered through Celite. The filtrate was concentrated and the crude material was purified on silica gel (hexanes/ethyl acetate) to give the title compound (2.9 g, 56%) as a white solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.31-7.40 (m, 2H), 7.21 (t, 1H), 7.04-7.11 (m, 2H), 4.51 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-ac9418daef9340c2b5ef82ebef08afa9
Source noteuspto-grants-2012_11