(+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one

Base Information

• Chemical Name: (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one
• CAS No.: 197306-30-2
• Molecular Formula: C₂₂H₂₈O
• Molecular Weight: 308.464

Synonyms:(+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one

Chemical Property of (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

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Technology Process of (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one

There total 3 articles about (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one 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: 56.0%

Methyltriphenylphosphonium bromide (1779-49-3) + (+)-(1R,2R,3R,4S,6R,7R)-1,6-dimethyl-4-acetyl-2-(2-methylphenyl)tricyclo[4.3.1.03,7]decan-9-one (197306-29-9) → (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.03,7]decan-9-one (197306-30-2)

Guidance literature:

With potassium 2-methylbutan-2-olate; In tert-Amyl alcohol; benzene; for 5h; Ambient temperature;

DOI:10.1021/jo9703360

Reference yield:

(1R,4R)-8-Methoxy-1,8-dimethyl-6-o-tolyl-bicyclo[2.2.2]oct-5-en-2-one → (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.03,7]decan-9-one (197306-30-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 67.7 percent / BBr₃ / CH₂Cl₂ / 1.5 h / -30 °C

2: 40 percent / Bu₃SnH, AIBN / benzene / 1 h / Heating

3: 56 percent / potassium tert-amyloxide / benzene; 2-methyl-butan-2-ol / 5 h / Ambient temperature

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; boron tribromide; potassium 2-methylbutan-2-olate; In tert-Amyl alcohol; dichloromethane; benzene;

DOI:10.1021/jo9703360

Reference yield:

(-)-(1R,4R,8S)-8-bromo-1,8-dimethyl-6-(2-methylphenyl)bicyclo[2.2.2]oct-5-en-2-one (197306-26-6) → (+)-(1R,2R,3S,4S,6R,7R)-1,6-dimethyl-4-isopropenyl-2-(2-methylphenyl)tricyclo[4.3.1.03,7]decan-9-one (197306-30-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 40 percent / Bu₃SnH, AIBN / benzene / 1 h / Heating

2: 56 percent / potassium tert-amyloxide / benzene; 2-methyl-butan-2-ol / 5 h / Ambient temperature

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; potassium 2-methylbutan-2-olate; In tert-Amyl alcohol; benzene;

DOI:10.1021/jo9703360

upstream raw materials:

Methyltriphenylphosphonium bromide

(+)-(1R,2R,3R,4S,6R,7R)-1,6-dimethyl-4-acetyl-2-(2-methylphenyl)tricyclo[4.3.1.0^3,7]decan-9-one

(-)-(1R,4R,8S)-8-bromo-1,8-dimethyl-6-(2-methylphenyl)bicyclo[2.2.2]oct-5-en-2-one

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