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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649524Generated: November 2, 2026

2-Nitrobenzenesulfonyl chloride → N-(Benzyloxy)-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1649524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantO-BenzylhydroxylamineHCID 102313—
SolventTetrahydrofuranHCID 8028—
ProductN-(Benzyloxy)-2-nitrobenzenesulfonamideHCID 983957893.2%

Reaction Steps

A solution of 96.4 g of O-benzylhydroxylamine in 80 ml of tetrahydrofuran was added to a solution of 86.8 g of o-nitrobenzenesulfonyl chloride in 400 ml of tetrahydrofuran at 5°-10°. After stirring at ambient temperature for 16 hours the solvent was evaporated. The residue was washed with water, filtered and dried to give 112.6 g of N-(phenylmethoxy)-2-nitrobenzenesulfonamide, m.p. 148°-151°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04417917
Source datasetuspto-grants-1983_11
ORD IDord-0eb95f8257334817bf38805635a23b9f
Source noteuspto-grants-1983_11