Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362275Generated: October 29, 2026

Triethylamine → N-(3-Chloro-2-propoxybenzyl)-N-methylacrylamide

https://huagongshe.com/reaction/1362275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant(3-Chloro-2-propoxybenzyl)methylamineHCID 66967022—
SolventDichloromethaneHCID 6344—
ProductN-(3-Chloro-2-propoxybenzyl)-N-methylacrylamideHCID 5927756589%

Reaction Steps

To a solution of (3-chloro-2-propoxybenzyl)methylamine (0.435 g, 2.04 mmol) in CH2Cl2 (18 mL) was added acryloyl chloride (0.18 mL, 2.24 mmol) drop-wise. After stirring for five minutes, triethylamine (0.531 mL, 2.24 mmol) was added. The solution was stirred under N2 for 18 h. The solution was diluted with CH2Cl2 (30 mL) and then washed with H2O (3×50 mL) and brine (2×100 mL), dried over Na2SO4, filtered and concentrated to yield the title compound (0.48 g, 89%) as a light yellow oil and as a mixture of amide rotamers: 1H NMR (500 MHz, CDCl3) δ 7.31-7.26 (m, 1H), 7.10-6.98 (m, 2H), 6.63-6.37 (m, 2H), 5.77-5.73 (m, 1H), 4.76-4.65 (m, 2H), 3.94-3.89 (m, 2H), 3.01 (s, 3H), 1.89-1.82 (m, 2H), 1.11-1.05 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-c48c4db3756444fcbd955a815608bb6f
Source noteuspto-grants-2011_02