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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870813Generated: October 29, 2026

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

https://huagongshe.com/reaction/870813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
SolventPyridineHCID 1049—
ProductN-(Benzyloxy)-2-nitrobenzenesulfonamideHCID 983957869.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 2-nitrobenzene-1-sulfonyl chloride (500 g, 2.26 mol) in pyridine (1500 mL) was added dropwise to a solution of O-benzylhydroxylamine hydrochloride (400 g, 2.51 mol) in pyridine (1500 mL) at 0° C. The reaction mixture was then stirred at 20° C. overnight. The mixture was concentrated in vacuum, diluted with DCM and washed with HCl (10%) three times. The combined organic layer was concentrated in vacuum and re-crystallized with DCM to afford N-(benzyloxy)-2-nitrobenzenesulfonamide (485 g, 62.6%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969570B2
Source datasetuspto-grants-2015_03
ORD IDord-558b40aed3a24b5c98686a41154af3a5
Source noteuspto-grants-2015_03