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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184350Generated: November 1, 2026

Ammonia → 3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enamide

https://huagongshe.com/reaction/2184350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxalyl chlorideHCID 65578—
Reactant3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enoic acidHCID 69289494—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enamideHCID 6928970165%

Reaction Conditions

Temperature0 °C

Reaction Steps

305 mg (1.07 mmol) of 3-[4-(3-fluoro-benzyloxy)-phenyl]-2-methyl-acrylic acid is dissolved in 8 ml of dichloromethane and one drop of dimethylformamide is added. The solution is cooled to 0° C. and treated dropwise with 676 mg (5.33 mmol) oxalyl chloride. The resulting solution is stirred at 0° C. for additional 30 minutes, then 2 hours at RT. Evaporation of the solvent leaves the crude acid chloride which is dissolved in 5 ml THF. This solution is slowly added under stirring to 10 ml of concentrated ammonia. The precipitate is filtered off and recrystallised from methanol to yield 199 mg (65%) of a colorless solid. MS: m/e=286.2 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900354B2
Source datasetuspto-grants-2005_05
ORD IDord-6e24374e65344b4b8ecacfa75efd3abc
Source noteuspto-grants-2005_05