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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407627Generated: November 1, 2026

Phenethylamine → N-Phenethylbenzenesulfonamide

https://huagongshe.com/reaction/2407627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
ProductN-PhenethylbenzenesulfonamideHCID 25413072.4%

Reaction Steps

To a stirred solution of 2-phenylethylamine (2 g, 16.5 mmol) in 105 ml DMF at room temperature was added Et3N (2.75 ml, 19.8 mmol). This mixture was stirred for 5 min, and then benzenesulfonyl chloride (2.3 ml, 18.1 mmol) was added at this temperature. The reaction was stirred for 2.5 h, and then, the mixture was evaporated to dryness and the crude was chromatographically purified over SiO2 using Hexane/AcOEt 60/40 as the eluant, yielding 3.12 g (72%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809584B2
Source datasetuspto-grants-2014_08
ORD IDord-f8c2a7f049a9471082f22abc058bd5a8
Source noteuspto-grants-2014_08