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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521637Generated: October 30, 2026

Triethylamine → 3-chloro-N-(3-fluorophenyl)propanamide

https://huagongshe.com/reaction/1521637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-FluoroanilineHCID 9742—
Reactant3-Chloropropionyl chlorideHCID 69364—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-chloro-N-(3-fluorophenyl)propanamideHCID 3555695—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-fluoroaniline (20 g, 0.180 mol) in dichloromethane (100 mL) was added triethylamine (21.816 g, 0.216 mol) and 3-chloropropanoyl chloride (17.18 mL, 0.180 mol) under cooling condition (0° C.) with constant stirring. Reaction mass was allowed to stir at room temperature for 12 h. The reaction mixture was diluted with water (300 mL) and extracted with dichloromethane (4×100 mL). The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under vacuum to obtain the title compound. 1H NMR (400 MHz, CDCl3) δ 7.51-7.48 (d, J=10.4 Hz, 1H), 7.42 (bs, 1H), 7.29-7.24 (dd, J=14.8 Hz, 8.0 Hz, 1H), 7.15-7.13 (d, J=8.0 Hz, 1H), 6.84-6.81 (t, J=6.8 Hz, 1H), 3.89-3.86 (t, J=6.4 Hz, 2H), 2.83-2.80 (t, J=6.4 Hz, 2H). MS (M+1): 201.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-b8a90603582e4bbf9ad7dbb5e9516811
Source noteuspto-grants-2015_07