Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611079Generated: October 30, 2026

Phenethylamine → Methanesulfonamide, N-(2-phenylethyl)-

https://huagongshe.com/reaction/1611079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
ProductMethanesulfonamide, N-(2-phenylethyl)-HCID 118569106.4%

Reaction Steps

To a 10° C. solution of phenethylamine (12.1 g, 0.100 mol) and triethylamine (11.1 g, 0.110 mol) in CH2Cl2 (50 mL) was added methanesulfonyl chloride (12.6 g, 0.110 mol) dropwise over 10 min. The solution was stirred at room temperature for 1.5 h and was then washed with 1N HCl (5×20 mL). The organic phase was directly concentrated to provide the intermediate title compound, (methylsulfonyl)(2-phenylethyl)amine, (21.2 g, 93.3%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984756B2
Source datasetuspto-grants-2006_01
ORD IDord-f41c03bc4a954803a615241c2fef61de
Source noteuspto-grants-2006_01