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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080507Generated: November 1, 2026

Ethanol → HCID 23114892, compound

https://huagongshe.com/reaction/2080507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58734278HCID 58734278—
SolventWaterHCID 962—
ProductHCID 23114892HCID 23114892—

Reaction Conditions

Temperature65 °C

Reaction Steps

To an ethanol (2 ml) solution of O-ethyl S-(6-trifluoromethylpyridin-3-yl) dithiocarbonate (160 mg, 0.60 mmol) was added a 1N aqueous sodium hydroxide solution (2 ml). The resulting mixture was stirred at 65° C. for 2 hours. After the reaction mixture was cooled to room temperature and then, water was added thereto. The resulting mixture was washed with dichloromethane. The water layer was acidified with 1N hydrochloric acid, and the product was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and then filtered. The filtrate was concentrated under reduced pressure to afford 6-trifluoromethylpyridine-3-thiol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932271B2
Source datasetuspto-grants-2011_04
ORD IDord-6cfbd175b49c47318f29348462c0e6da
Source noteuspto-grants-2011_04