関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | (2,4-Difluoro-phenyl)-hydrazine | HCID 588958 | — |
| 反応物 | Cyclohexanone, 4-(1-piperidinyl)- | HCID 12361785 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole | HCID 12361824 | — |
反応手順
A solution of 10.2 g. of 4-(1-piperidyl)-cyclohexanone, 8.1 g. of 2,4-difluorophenylhydrazine, and 11 g. of methanesulfonic acid in 100 ml. of absolute ethyl alcohol was heated under reflux for 12 hours, cooled, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was treated in ether with 10% potassium hydroxide solution and the ether extract was washed with water, dried, and treated with hydrogen chloride in ethyl alcohol (excess HCl was avoided). The resulting gummy precipitate was separated by decantation and suspended in boiling isopropyl alcohol. The hot mixture was filtered to give, after recrystallization from absolute ethyl alcohol, 4.5 g. of 3-(1-piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. > 290° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04062864 |
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| 出典データセット | uspto-grants-1977_12 |
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| ORD ID | ord-babb356db7d24e0ebcc7209ba8042f2f |
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| 出典メモ | uspto-grants-1977_12 |
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