HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917912Generated: November 3, 2026
Potassium Hydroxide → HCID 21524263, compound
https://huagongshe.com/reaction/917912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21524245 | HCID 21524245 | — |
| Solvent | Triethylene Glycol | HCID 8172 | — |
| Product | HCID 21524263 | HCID 21524263 | 78.6% |
Reaction Steps
A mixture of 6 g of 4-oxo-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid, 4 g of hydrazine hydrate, 6.4 g of potassium hydroxide and 40 ml of triethyleneglycol is heated for 2 hours at 130°-140°C. Then, while distilling off a mixture of hydrazine and water, the temperature is raised to 195°C and the batch is stirred until nitrogen is no longer being given off, then diluted with 50 ml of water, acidified with concentrated hydrochloric acid and the mixture is extracted with ethyl acetate and the ethyl acetate is evaporated. The resulting crude product is recrystallized from toluene, to yield 4.5 g of 6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid melting at 119°-120°, of the formula ##SPC10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03968142 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-0665af11146a45b4be585f1c6ffa3267 |
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| Source note | uspto-grants-1976_07 |
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