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Allyl bromide → HCID 23339063、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamide | HCID 162188 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | HCID 23339063 | HCID 23339063 | — |
反応手順
To a stirring solution of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 3.8 parts of N-N-diethylethanamine in 200 parts of benzene are added portionwise 5 parts of 3-bromo-1-propene. After the addition is complete, the whole is heated for 21 hours at a temperature between 50°-60° C. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, dried over potassium carbonate and evaporated. The oily residue is converted into the hydrochloride salt in 1,1'-oxybisethane and 2-propanone, yielding 4 parts of N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochloride; mp. 225.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04225606 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-13f2a08e8f854d1fbf80096f4777ac60 |
| 出典メモ | uspto-grants-1980_09 |