HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866931Generated: October 30, 2026
Ethanol → 2-Trifluoromethyl-10,11-dihydrodibenzo[b,f]thiepin-9-carboxylic acid
https://huagongshe.com/reaction/866931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Trifluoromethyl-9-cyano-10,11-dihydrodibenzo[b,f]thiepin | HCID 12687122 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Trifluoromethyl-10,11-dihydrodibenzo[b,f]thiepin-9-carboxylic acid | HCID 12687124 | — |
Reaction Steps
To 1g of potassium hydroxide dissolved in 1ml of water and 4ml of ethanol was added 106mg 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101667 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-8311df88ee12448f9915213e96a8cecb |
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| Source note | uspto-grants-1978_07 |
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