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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261564Generated: November 1, 2026

Ethanol → 2-Trifluoromethyl-10,11-dihydrodibenzo[b,f]thiepin-9-carboxylic acid

https://huagongshe.com/reaction/261564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant2-Trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f]thiepinHCID 12687122—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Trifluoromethyl-10,11-dihydrodibenzo[b,f]thiepin-9-carboxylic acidHCID 12687124—

Reaction Steps

To 1 g of potassium hydroxide dissolved in 1 ml of water and 4 ml of ethanol was added 106 mg of 2-trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f] thiepin and the resulting mixture was refluxed for 24 hrs. After cooling, to this was added 4% sodium hydroxide solution and ether. After shaking, the aqueous layer was separated, acidified by adding conc. hydrochloric acid and extracted with chloroform. Extract was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 87 mg (77.3% of yield) of the desired product as colorless powder. This was recrystallized from the mixed solvent of benzene and n-hexane to afford 2-trifluoromethyl-10,11-dihydrodibenzo[b,f]thiepin-9-carboxylic acid having a melting point of 178.5° to 179.5° C. as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166127
Source datasetuspto-grants-1979_08
ORD IDord-15f2c54e29f3451186675c8ac7dc2236
Source noteuspto-grants-1979_08