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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078639Generated: October 29, 2026

Ammonium Hydroxide → 2-(Phenylmethoxy)ethanesulfonamide

https://huagongshe.com/reaction/2078639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Benzyloxy-ethanesulfonyl chlorideHCID 64179623—
SolventDichloromethaneHCID 6344—
Product2-(Phenylmethoxy)ethanesulfonamideHCID 64200908—

Reaction Steps

To a 28% ammonium hydroxide (10 ml) was added dropwise 2-(benzyloxy)ethanesulfonyl chloride (4.1 g) in dichloromethane (10 ml) over 10 minutes under ice-cooling. The mixture was stirred at ambient temperature overnight. The organic layer was separated and the aqueous layer was extracted with dichloromethane/methanol (5/1). The combined organic layer was dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=50/50) to give 2-(benzyloxy)ethanesulfonamide (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928264B2
Source datasetuspto-grants-2011_04
ORD IDord-b88c54b646644b2da5bf35f1e027b8dc
Source noteuspto-grants-2011_04