(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

Base Information

Chemical Name:(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile
CAS No.:272767-04-1
Molecular Formula:C₁₆H₂₃NO₂
Molecular Weight:261.364
Hs Code.:

Synonyms:(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

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Chemical Property of (1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

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Technology Process of (1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

There total 5 articles about (1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 94.0%

: 78-94-4,25038-87-3
methyl vinyl ketone

: 272767-14-3
(1R,6R)-6-isopropenyl-3,3-dimethyl-2-oxo-cyclohexanecarbonitrile

: 272767-04-1
(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

Guidance literature:: With sodium methylate; In methanol; benzene; for 3h;
DOI:10.1016/S0040-4020(00)00110-1

Reference yield:

: 69153-92-0
(5R)-5-isopropenyl-2,2-dimethylcyclohexanone

: 272767-04-1
(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / NaH / diethyl ether / 20 °C

2: NH₂OH*HCl; NaOAc / CHCl₃; ethanol / 48 h

3: NaOMe / methanol; diethyl ether / 24 h

4: 94 percent / NaOMe / benzene; methanol / 3 h

With hydroxylamine hydrochloride; sodium methylate; sodium acetate; sodium hydride; In methanol; diethyl ether; ethanol; chloroform; benzene; 1: Formylation / 2: Condensation / 3: Ring cleavage / 4: Michael addition;
DOI:10.1016/S0040-4020(00)00110-1

Reference yield:

: 272766-93-5
(4S)-4-isopropenyl-7,7-dimethyl-4,5,6,7-tetrahydrobenzo[d]isoxazole

: 272767-04-1
(1S,6S)-6-isopropenyl-3,3-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: NaOMe / methanol; diethyl ether / 24 h

2: 94 percent / NaOMe / benzene; methanol / 3 h

With sodium methylate; In methanol; diethyl ether; benzene; 1: Ring cleavage / 2: Michael addition;
DOI:10.1016/S0040-4020(00)00110-1