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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287765Generated: October 26, 2026

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

https://huagongshe.com/reaction/1287765

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 numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-9ebbcc857bdd49c188d533c1222f2180
Source noteuspto-grants-1976_10