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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052639Generated: October 30, 2026

N-(3-methoxy-5-nitrophenyl)methanesulfonamide → N-(3-amino-5-methoxyphenyl)methanesulfonamide

https://huagongshe.com/reaction/1052639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-methoxy-5-nitrophenyl)methanesulfonamideHCID 68836539—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductN-(3-amino-5-methoxyphenyl)methanesulfonamideHCID 6884023099%

Reaction Conditions

Temperature40 °C

Reaction Steps

N-(3-Methoxy-5-nitrophenyl)methanesulfonamide (3 g, 11.82 mmol) was treated with iron powder (3.3 g, 59.09 mmol) in acetic acid (120 ml) and stirred at 40° C. for 2 h. The crude was then filtered over Celite and the solvent was removed in vacuum. A mixture of a solution of sodium bicarbonate 4% and ethyl acetate was added and the resulting mixture was filtered over Celite. The organic phase was washed with water and brine, dried over magnesium sulphate and the solvent was remove to give 2.53 g (86% yield) of the title compound as a dark solid, that was used in the next step without further purification. Purity 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388189B2
Source datasetuspto-grants-2016_07
ORD IDord-78a0fc98293c40718cba05cd5a33f48c
Source noteuspto-grants-2016_07