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HRID 268195作成日:2026年10月27日

Ammonia → 3-Methylcyclohexanone

https://huagongshe.com/reaction/268195

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物Hydrogen PeroxideHCID 784—
反応物3-MethylcyclohexanoneHCID 11567—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物3-MethylcyclohexanoneHCID 11567—
生成物3-MethylcaprolactamHCID 581216—

反応手順

3,3'-Dimethyl-1,1'-peroxydicyclohexylamine (10 g.) derived from 3-methylcyclohexanone, hydrogen peroxide and ammonia, and probably a mixture of stereoisomers was added to a solution of sodium methoxide in methanol (2 g. sodium in 40 c.c. methanol) and the mixture heated under reflux for 2 hours; only a small amount of peroxide remained unreacted. The solution was cooled, diluted with water, neutralised with hydrochloric acid and extracted with chloroform. Distillation of the chloroform extract gave 3-methylcyclohexanone (4.7 g.), methylcaprolactam (4.1 g), b.p. 145°-150°/15 mm., and residue (0.5 g.). Examination of the methylcaprolactam fraction by N.M.R. spectroscopy showed it to be a mixture of 3- and 5-methyl-caprolactam; on storage this fraction crystallized and several recrystallisations yielded the 3-methylcaprolactam, m.p. 87°-100°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03947406
出典データセットuspto-grants-1976_03
ORD IDord-5eaa7c71fcff430a8a59d0620b31fc51
出典メモuspto-grants-1976_03