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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232353Generated: November 1, 2026

HCID 13922872, compound → HCID 13922873, compound

https://huagongshe.com/reaction/2232353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13922872HCID 13922872—
SolventMethanolHCID 887—
SolventPotassium HydroxideHCID 14797—
ProductHCID 13922873HCID 1392287341%

Reaction Steps

A solution of 5-acetoxymethyl-2-sulfamoylbenzo[b]thiophene (5.6 g, 19.6 mmol) in 25 ml of 1M aqueous KOH and 25 ml of methanol was stirred at room temperature for 2 hours and at reflux for 21/2 hours. The mixture was filtered and the methanol was removed in vacuo. The remaining aqueous suspension was acidified with excess 6N HCl and the solid was filtered, washed with ice water and dried. The crude material (3.1 g) was chromatographed on silica gel using 5% (V/V) methanol in chloroform. Product was obtained as a yellow solid (1.85 g), m.p. 174°-176° C. Yield 41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788192
Source datasetuspto-grants-1988_11
ORD IDord-29f2f0d6c62e48549045253834f94c3e
Source noteuspto-grants-1988_11