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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592329Generated: October 31, 2026

Triethylamine → N-cyclopropyl-3-(4-fluorophenyl)propanamide

https://huagongshe.com/reaction/1592329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantCyclopropylamineHCID 69828—
Reactant3-(4-Fluorophenyl)propionic acidHCID 136302—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-cyclopropyl-3-(4-fluorophenyl)propanamideHCID 5692328276.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-(4-fluorophenyl)propionic acid (5 g, 31 mmoles) and 0.1 mL of dimethylformamide in 50 mL of anhydrous CH2Cl2 at 0° C. was added oxalyl chloride (2.84 mL, 32.6 mmoles) and the mixture was stirred for 1 hour at 0° C. and for 1 hour at room temperature. After cooling to 0° C. were added cyclopropylamine (2.6 mL, 37.2 mmoles) and triethylamine (6.5 mL, 46.5 mmoles), and the mixture was stirred for 1 hour while warming to room temperature gradually. Then water was added and the product was extracted with CH2Cl2. The extract was washed with water, dried over MgSO4 and evaporated to give a solide residue. It was recrystallized from CH2Cl2 and hexane to give 4.94 g of N-cyclopropyl-3-(4-fluorophenyl)propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291744B2
Source datasetuspto-grants-2007_11
ORD IDord-669fca97987a4db8868c7a78d014de78
Source noteuspto-grants-2007_11