N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

Base Information

Chemical Name:N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide
CAS No.:132292-39-8
Molecular Formula:C₁₆H₂₅NO₃
Molecular Weight:279.379
Hs Code.:

Synonyms:N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

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Chemical Property of N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

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Technology Process of N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

There total 3 articles about N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide 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: 83.0%

: 132292-33-2
C₁₆H₂₃NO₂

: 132292-39-8
N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

Guidance literature:: With sodium hydrogen sulfate; In dichloromethane; at 20 ℃; for 168h;
DOI:10.1055/s-1990-27073

Reference yield:

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 132292-39-8
N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / CH₂Cl₂ / 24 h / 20 °C

2: 83 percent / aq NaHSO₄ / CH₂Cl₂ / 168 h / 20 °C

With sodium hydrogen sulfate; In dichloromethane;
DOI:10.1055/s-1990-27073

Reference yield:

: 110174-72-6
2-(1-piperidinocycloprop-1-yl)-5,5-dimethyl-3-oxocyclohex-1-en-1-yl acetate

: 132292-39-8
N-tert-butyl-1-(2-hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / CH₂Cl₂ / 24 h / 20 °C

2: 83 percent / aq NaHSO₄ / CH₂Cl₂ / 168 h / 20 °C

With sodium hydrogen sulfate; In dichloromethane;
DOI:10.1055/s-1990-27073