HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248161Generated: October 31, 2026
Potassium Hydroxide → HCID 12909376, compound
https://huagongshe.com/reaction/1248161
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12909378 | HCID 12909378 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12909376 | HCID 12909376 | 94.5% |
Reaction Steps
A solution of 1.24 g of (-)-ethyl 5-(1-methyl-4-piperidylidene)-5H-dibenzo[a,d]cycloheptene-3-carboxylate and 4.12 ml of 2N potassium hydroxide in 55 ml of methanol was stirred at room temperature for seven days. The methanol was removed by evaporation at 25°. The residue was dissolved in water and extracted with 50 ml of ether. The clear, colorless aqueous phase was acidified with glacial acetic acid. The white precipitate that formed was removed by filtration, and washed thoroughly with water. After drying at 100° in vacuo, 1.08 g of (-)-5-(1-methyl-4-piperidylidene)-5H-dibenzo[a,d]cycloheptene-3-carboxylic acid was obtained, m.p. 300°-305°; [α]58925 -180°; [α]57825 -194°; [α]54625 -239°; [α]43625 -675°; (c=0.004968 g/ml 0.10 NHCl). Rf : 0.70 (fluorescent silica gel, n-butanol/acetic acid/water (5:2:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04522821 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-d92577c5ccc44e74af82b9f826fb5dfc |
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| Source note | uspto-grants-1985_06 |
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