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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082890Generated: October 31, 2026

Water → 5-(Aminomethyl)-3-(butylamino)-2-phenoxybenzene-1-sulfonamide

https://huagongshe.com/reaction/2082890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(Butylamino)-5-cyano-2-phenoxybenzene-1-sulfonamideHCID 53898140—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(Aminomethyl)-3-(butylamino)-2-phenoxybenzene-1-sulfonamideHCID 54039296—

Reaction Steps

To a stirred mixture of lithium aluminum hydride (5.0 g) and 1,2-dimethoxyethane (100 ml) a solution of 3-n-butylamino-4-phenoxy-5-sulfamylbenzonitrile (15 g) in dry 1,2-dimethoxyethane (150 ml) is during about 1 hour at 100° C. dropwise added, and the mixture is stirred and refluxed for a further 16 hours. After cooling, ethyl acetate (10 ml) followed by water (20 ml) are very cautiously added dropwise, whereafter the mixture is stirred for a further 30 minutes. It is then heated on a steam-bath and filtered hot; the filter-cake is carefully washed with hot 2-methoxyethanol (3 portions of 50 ml). The combined filtrates are evaporated in vacuo to yield crude 3-n-butylamino-4-phenoxy-5-sulfamylbenzylamine. After recrystallization from 2-methoxyethanol it is obtained with a melting point of 197°-198° C. The material (IR, analysis) is identical with the material prepared as in Example 289.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082851
Source datasetuspto-grants-1978_04
ORD IDord-aa2878dd7a734d3db809c5c1f4f2bb61
Source noteuspto-grants-1978_04