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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613858Generated: November 4, 2026

4-Fluorobenzoyl chloride → 2-(4-Fluorophenyl)-6-hydroxybenzothiazole

https://huagongshe.com/reaction/1613858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant2-Amino-5-methoxybenzene-1-thiolHCID 235509—
Reactant2-(4-Fluorophenyl)-6-methoxy-1,3-benzothiazoleHCID 12179987—
Product2-(4-Fluorophenyl)-6-hydroxybenzothiazoleHCID 16734166—

Reaction Steps

The procedure set out in Example 7 is repeated using 2-amino-5-methoxybenzenethiol and 4-fluorobenzoyl chloride. The reaction yields a mixture of the title compound and 2-(4-fluorophenyl)-6-methoxybenzothiazole. The mixture is treated with excess boiling 48 percent HBr for one hour to convert the latter product to the title compound. The solution is filtered and the precipitate is recrystallized from ethanol and water. The overall yield is 80.3 percent based on the initial amount of benzenethiol. A recrystallized product melts at about 221° C.-223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194562
Source datasetuspto-grants-1993_03
ORD IDord-33025c69060548439d752e3ce8a2fe1f
Source noteuspto-grants-1993_03