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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918653Generated: October 26, 2026

3-Nitro-4-phenoxy-5-sulphamyl-benzamide → 3-Amino-4-phenoxy-5-sulphamyl-benzamide

https://huagongshe.com/reaction/918653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-4-phenoxy-5-sulphamyl-benzamideHCID 21506072—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
Product3-Amino-4-phenoxy-5-sulphamyl-benzamideHCID 21506074—

Reaction Steps

To a suspension of 3-nitro-4-phenoxy-5-sulphamyl-benzamide (2.4 g) in water (25 ml) 1N lithium hydroxide (10 ml) was added. The resulting solution was hydrogenated at room temperature and at 1.1 atmospheres hydrogen pressure after addition of Pd-on-carbon catalyst (0.2 g catalyst containing 10% Pd). After the hydrogen uptake had become negligible, the catalyst was removed by filtration, and the filtrate was then adjusted to pH 7.5 by addition of 4N hydrochloric acid. The precipitated 3-amino-4-phenoxy-5-sulphamyl-benzamide was isolated and dried in vacuo. The compound was obtained with a melting point of 291°-292°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03971819
Source datasetuspto-grants-1976_07
ORD IDord-8bd61c11c0be4f13b8c5ff288c7c7844
Source noteuspto-grants-1976_07