HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648936Generated: October 31, 2026
Potassium Hydroxide → HCID 20481335, compound
https://huagongshe.com/reaction/1648936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20481315 | HCID 20481315 | — |
| Reactant | HCID 20481318 | HCID 20481318 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20481335 | HCID 20481335 | — |
Reaction Steps
10 gm (0.034 mol) of an isomer mixture consisting of diethyl 5,6,7,8-tetrahydro-4H-thieno[2,3-d]azepine-2,6-dicarboxylate and diethyl 5,6,7,8-tetrahydro-4H-thieno[3,2-c]azepine-2,5-dicarboxylate were refluxed for 4 hours in a solution of 2.8 gm (0.05 mol) of potassium hydroxide in 150 ml of absolute ethyl alcohol. Then, the mixture was concentrated by evaporation in vacuo, the residue was taken up in water and extracted three times with ether. The ether extracts were discarded, and the aqueous phase was acidified with concentrated hydrochloric acid. It was extracted several times with ether, and the combined ether phases were washed with water and dried over sodium sulfate. After the ether had been distilled off, 9.2 gm of a yellowish oil remained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04414225 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-0ca894f8e01a464f9f547f13a04e6299 |
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| Source note | uspto-grants-1983_11 |
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