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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505622Generated: October 31, 2026

Triethylamine → HCID 33037887, compound

https://huagongshe.com/reaction/1505622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
Reactant(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 852999—
SolventDichloromethaneHCID 6344—
ProductHCID 33037887HCID 3303788771%

Reaction Steps

Phenylmethanesulfonyl chloride (28.1 g, 147.7 mmol) was added into a solution of (S)-1-(4-bromophenyl)ethanamine (28.0 g, 140.7 mmol) and triethylamine (21.3 g, 211.1 mmol) in dichloromethane (400 mL) drop wise at 0° C. The reaction mixture was stirred at ambient temperature for 12 hours. The reaction solution was then washed with dilute aqueous HCl, saturated aqueous NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered, and concentrated to provide the title compound (35.3 g, 71% yield) as pale yellow solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216988B2
Source datasetuspto-grants-2015_12
ORD IDord-0d7418ab281e4c31bd501a146161c214
Source noteuspto-grants-2015_12