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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875097Generated: November 4, 2026

Ammonia → 3-{[3-(Aminomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrile

https://huagongshe.com/reaction/1875097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
Reactant3-{[3-(Bromomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrileHCID 68485368—
SolventTetrahydrofuranHCID 8028—
Product3-{[3-(Aminomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrileHCID 6848554786%

Reaction Steps

A 7M solution of ammonia in MeOH (45.8 mL, 321 mmol) was added to a solution of 3-{[3-(bromomethyl)-2,6-difluorophenyl]oxy}-5-chlorobenzonitrile (2.3 g, 6.41 mmol) in THF (30 mL) at RT. The reaction was capped and stirred for 16 h at RT then concentrated to dryness under vacuum. Ethyl acetate (200 mL) and saturated aqueous NaHCO3 solution (300 mL) were added. The organic layer was separated, washed with saturated aqueous NaHCO3 solution (2×200 mL), water (200 mL), brine (200 mL), dried over Na2SO4, filtered and concentrated to give a white solid. The crude product was purified on silica gel (10% MeOH/DCM) to give the title compound (1.63 g, 86%) as a white solid (N4011-13-100). 1H NMR (400 MHz, DMSO-d5) δ ppm 7.82 (s, 1H), 7.40-7.66 (m, 3H), 7.31 (t, 1H), 3.75 (s, 2H), 1.86 (br. s., 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-77064fd2031f46eb892b06beb08e3c49
Source noteuspto-grants-2012_11