Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237544Generated: October 25, 2026

Triethylamine → N-(2-(4-bromo-3,5-dimethylphenoxy)ethyl)methanesulfonamide

https://huagongshe.com/reaction/237544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(4-Bromo-3,5-dimethylphenoxy)ethanamineHCID 22688749—
SolventDichloromethaneHCID 6344—
ProductN-(2-(4-bromo-3,5-dimethylphenoxy)ethyl)methanesulfonamideHCID 86697208—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 2-(4-bromo-3,5-dimethylphenoxy)ethanamine (100 mg) and triethylamine (63 μL) in dichloromethane (2 mL) is added methanesulfonyl chloride (32 μL). The mixture is stirred for 2 hours at 0° C. Then the mixture is partitioned between dichloromethane and water. The organic phase is separated, washed with brine and dried (MgSO4). The solvent is evaporated and the residue is purified by HPLC on reversed phase to give the title compound. Yield: 90 mg; LC (method 7): tR=1.01 min; Mass spectrum (ESI+): m/z=322 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642585B2
Source datasetuspto-grants-2014_02
ORD IDord-5bdcf8c67df74aa5851c07702d842fbb
Source noteuspto-grants-2014_02