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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356823Generated: October 25, 2026

Methylamine → N-methyl-3-phenylprop-2-en-1-amine

https://huagongshe.com/reaction/1356823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantBenzene, (3-chloro-1-propenyl)-HCID 94242—
SolventMethanolHCID 887—
ProductN-methyl-3-phenylprop-2-en-1-amineHCID 18918383%

Reaction Steps

Triethylamine (0.66 g; 6.55 mmol) was added to 40% solution of methylamine in methanol (20 ml). While the mixture was stirred at room temperature, cinnamyl chloride (1.00 g; 6.55 mmol) was added dropwise. After completion of the addition, the mixture was stirred for 20 hours at room temperature, and excess methylamine and methanol were removed under reduced pressure. The residue was taken up in a mixture of diethyl ether and 2N hydrochloric acid (100 ml-100 ml), and the aqueous layer was neutralized with aqueous sodium hydroxide solution, followed by extraction with chloroform (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution and then with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, to thereby yield 0.80 g of the target compound as yellow oily matter (yield: 83.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586633B1
Source datasetuspto-grants-2003_07
ORD IDord-6ccf9d5ec7cd452e89cc8c4b5df5ac97
Source noteuspto-grants-2003_07