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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390048Generated: October 31, 2026

Water → 3-Amino-5-(hydroxymethyl)-2-phenoxybenzene-1-sulfonamide

https://huagongshe.com/reaction/1390048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 3-amino-4-phenoxy-5-sulfamoylbenzoateHCID 20294607—
ReactantAluminium lithium hydrideHCID 21226445—
SolventAcetic AcidHCID 176—
Solvent1,4-DioxaneHCID 31275—
Product3-Amino-5-(hydroxymethyl)-2-phenoxybenzene-1-sulfonamideHCID 54036191—

Reaction Steps

To a stirred mixture of lithium aluminium hydride (12.5 g) and dry dioxane (250 ml), a solution of ethyl 3-amino-4-phenoxy-5-sulfamylbenzoate (50 g) in dry dioxane (250 ml) is dropwise added at 90° C. during about one hour. After additional stirring and heating for 3 hours, the mixture is cooled, and ethyl acetate (25 ml) followed by water (50 ml) and 4 N acetic acid (310 ml) are very cautiously added dropwise. The solvents are thereafter removed in vacuo, and the residue is extracted with ethyl acetate (1 liter). The insoluble inorganic material is removed by filtration, and the filtrate is washed with aqueous sodium hydrogen carbonate and with water, and is then dried in the presence of magnesium sulphate. After filtration, the solvent is removed in vacuo to yield crude 3-amino-4-phenoxy-5-sulfamylbenzyl alcohol. After recrystallization from aqueous ethanol it is obtained with a melting point of 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04247550
Source datasetuspto-grants-1981_01
ORD IDord-d2836dadc55c4b7bb35eecb9d9b34f85
Source noteuspto-grants-1981_01