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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449115Generated: November 1, 2026

Ethanol → 1,2-Benzisothiazol-4-ol, 7-amino-

https://huagongshe.com/reaction/1449115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
Reactant7-Acetamino-4-acetoxy-1,2-benzisothiazoleHCID 20349941—
SolventAcetic AcidHCID 176—
Solvent1-PropanolHCID 1031—
Product1,2-Benzisothiazol-4-ol, 7-amino-HCID 135617187—

Reaction Steps

This reduction is as a rule carried out under atmospheric pressure or in a closed vessel under superatmospheric pressure, with or without simultaneous heating. The reaction may be carried out in the presence of a diluent or solvent, for example, a lower alcohol, e.g. methanol, ethanol or preferably propanol, or in the acid required for the reduction, preferably in acetic acid, or in the acylating reaction medium of acetic acid and acetic anhydride, described above, in which 7-acetamino-4-acetoxy-1,2-benzisothiazole is obtained. 7-Acetamino-4-acetoxy-1,2-benzisothiazole can subsequently be deacylated in the above manner to give 7-amino-4-hydroxy-1,2-benzisothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189433
Source datasetuspto-grants-1980_02
ORD IDord-38f6917caac942a9a95e10acc735d2e3
Source noteuspto-grants-1980_02