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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569803Generated: October 30, 2026

N-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamide → 2-amino-N-(3,4-dichlorobenzyl)benzenesulfonamide

https://huagongshe.com/reaction/569803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamideHCID 1000717—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product2-amino-N-(3,4-dichlorobenzyl)benzenesulfonamideHCID 372802792.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of N-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamide (4 g) and iron (2 g) in acetic acid (30 ml) was stirred at 100° C. for 45 minutes. After cooling, the iron was filtered off. The filtrate was made alkaline with a diluted aqueous sodium hydroxide and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. Recrystallization from ethyl ether gave 2-amino-N-(3,4-dichlorobenzyl)benzenesulfonamide (3.40 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734419
Source datasetuspto-grants-1988_03
ORD IDord-bb18963c1b3f4082bd9183a4a7b60aaa
Source noteuspto-grants-1988_03