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Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-(4-chlorophenyl)piperidin-4-amine | HCID 7183033 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine | HCID 23339007 | — |
反応手順
To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20h. 30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04157393 |
| 出典データセット | uspto-grants-1979_06 |
| ORD ID | ord-98e53cc324e84b83a60aa09d13d4d66e |
| 出典メモ | uspto-grants-1979_06 |