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HRID 223639作成日:2026年10月24日

Cyclohexanone → N-cyclohexylidene-(2-methylpropenylamine)

https://huagongshe.com/ja/reaction/223639

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanoneHCID 7967—
反応物4-Pentenoic acidHCID 61138—
反応物2-MethylallylamineHCID 76141—
生成物N-cyclohexylidene-(2-methylpropenylamine)HCID 20436157—

反応手順

The procedure described in Example 1(a) is repeated, except that 302.5 g (2 mols) of N-cyclohexylidene-(2-methylpropenylamine) and 250 g (4.62 mols) of 1,3-butadiene are used. Distillation yields 382 g (1.48 mols) of 3,3-dimethyl-12,12-pentamethylene-1-aza-1,5,9-cyclododecatriene; boiling point 96° C./4 Pa; nD20 =1.5116. The N-cyclohexylidene-(2-methylpropenylamine) was prepared from cyclohexanone and methallylamine, with subsequent isomerisation of the reaction product with potassium tert.-butylate; boiling point 96° C./1,700 Pa; nD20 =1.5160.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04355177
出典データセットuspto-grants-1982_10
ORD IDord-279acf50c4024af1a52e52c5c1cf3d06
出典メモuspto-grants-1982_10