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Benzylamine → 3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatriene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzylamine | HCID 7504 | — |
| 反応物 | 2-Ethylhex-2-Enal | HCID 12582 | — |
| 反応物 | N-benzylidene-(2-ethyl-1-hexenylamine) | HCID 56636874 | — |
| 生成物 | 3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatriene | HCID 54523241 | — |
反応手順
The procedure described in Example 1(a) is repeated, except that 215.3 g (1 mol) of N-benzylidene-(2-ethyl-1-hexenylamine) [1-phenyl-4-ethyl-4-n-butyl-2-aza-1,3-butadiene; prepared by reacting benzylamine with 2-ethyl-hexenal and then isomerising the reaction product with potassium tert.-butylate; boiling point 90° C./7 Pa; nD20 =1.5630] are used. Distillation yields 288 g (0.891 mol) of 3-n-butyl-3-ethyl-12-phenyl-1-aza-1,5,9-cyclododecatriene; boiling point 130° C./2 Pa; nD20 =1.5296.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04355177 |
| 出典データセット | uspto-grants-1982_10 |
| ORD ID | ord-099217fb9a2d4c969136b0514f5ca373 |
| 出典メモ | uspto-grants-1982_10 |