(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

Base Information

Chemical Name:(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane
CAS No.:1616253-74-7
Molecular Formula:C₁₉H₂₈O₂
Molecular Weight:288.43
Hs Code.:

Synonyms:(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

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Technology Process of (1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

There total 4 articles about (1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane 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: 74.0%

: 1616253-67-8
2-((1R,6R)-6-isopropyl-3-methylcyclohex-2-enyl)-1-methoxy-3,5-dimethylbenzene

: 1616253-74-7
(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1021/jo5006069

Reference yield:

: 108-68-9,50356-23-5
3,5-Dimethylphenol

: 1616253-74-7
(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

Guidance literature:: Multi-step reaction with 3 steps

1: toluene-4-sulfonic acid / toluene / 3 h / 20 °C / Inert atmosphere

2: potassium carbonate / acetone / 4 h / Reflux

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C / Inert atmosphere

With potassium carbonate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetone; toluene;
DOI:10.1021/jo5006069

Reference yield:

: 4221-98-1
(R)-5-isopropyl-2-methylcyclohexa-1,3-diene

: 1616253-74-7
(1R,4R,5S,6S)-4-isopropyl-1-methyl-5-(2-methoxy-4,6-dimethylphenyl)oxabicyclo[4.1.0]heptane

Guidance literature:: Multi-step reaction with 3 steps

1: toluene-4-sulfonic acid / toluene / 3 h / 20 °C / Inert atmosphere

2: potassium carbonate / acetone / 4 h / Reflux

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C / Inert atmosphere

With potassium carbonate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetone; toluene;
DOI:10.1021/jo5006069