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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739452Generated: November 2, 2026

Thioglycolic Acid → 5-Fluoro-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/1739452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
Reactant2,5-DifluorobenzaldehydeHCID 137663—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
Product5-Fluoro-1-benzothiophene-2-carboxylic acidHCID 90143980.1%

Reaction Conditions

Temperature125 °C

Reaction Steps

In a glass pressure bottle, 2,5-difluorobenzaldehyde (11 ml, 0.1 mol) was added to a solution of 2-mercaptoacetic acid (9 ml) in potassium hydroxide (16.5 g) and water (155 ml). The bottle was then sealed and heated in a hot oil bath to 125±5° C. for 1.25 hours. The bottle was then removed from the hot oil bath and cooled. A pale yellow precipitate was obtained in the bottle. At ambient temperature, the bottle was opened and sufficient water was added to dissolve the precipitate. The resultant aqueous material was washed with ether and then acidified with hydrochloric acid to produce a pale yellow solid. The pale yellow solid was collected on a filter, washed with water and dried, to produce 15.5 g of 5-fluoro-2-benzo-[b]thiophenecarboxylic acid (80.1% yield, mp>300° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965749
Source datasetuspto-grants-1999_10
ORD IDord-8597088b936b4e00b8463565dad44c73
Source noteuspto-grants-1999_10