Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749457Generated: October 30, 2026

Ethylamine → (2S)-N-ethyl-2-(4-fluorophenyl)pent-4-enamide

https://huagongshe.com/reaction/749457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant(S)-2-(4-fluorophenyl)pent-4-enoyl chlorideHCID 15536025—
SolventDichloromethaneHCID 6344—
Product(2S)-N-ethyl-2-(4-fluorophenyl)pent-4-enamideHCID 6897878659%

Reaction Steps

A stream of ethylamine was introduced to ice-cooled CH2Cl2 (5 mL) until 350 mg gas had been consumed. A solution of (2S)-2-(4-fluorophenyl)pent-4-enoyl chloride (0.24 g in 5 mL of CH2Cl2, 1.1 mmol) was added dropwise. The mixture was stirred at room temperature for 1 h and then diluted with CH2Cl2 (10 mL). The solution was washed with aqueous solutions of KHSO4 (8 mL, 1M), NaOH (8 mL, 1M) and then brine. The organic solution was dried over Na2SO4 and then the solvent was evaporated. There was obtained 0.15 g (59%) of (2S)-N-ethyl-2-(4-fluorophenyl)pent-4-enamide. 1H NMR (500 MHz, CDCl3): 1.1 (t, 3H), 2.5 (m, 1H), 2.8-3.0 (m, 2H), 3.2-3.4 (m, 3H), 5.0-5.1 (m, 2H), 5.6-5.8 (m, 1H), 7.0 (t, 2H), 7.3 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402581B2
Source datasetuspto-grants-2008_07
ORD IDord-dbc78ff35b2941078b77e2bcd200f3c8
Source noteuspto-grants-2008_07