Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

Base Information

Chemical Name:Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester
CAS No.:308258-36-8
Molecular Formula:C₁₈H₃₀O₂
Molecular Weight:278.435
Hs Code.:

Synonyms:Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

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Chemical Property of Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

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Technology Process of Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

There total 2 articles about Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester 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:

: 52690-42-3
(-)-4-<(1S,6R)-2,2,6-trimethyl-6-vinylcyclohexyl>butan-2-one

: 308258-36-8
Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: O₃; vinyl acetate / CH₂Cl₂ / -78 °C

1.2: 57 percent / hexane / 12 h / Heating

2.1: 82 percent / tetrahydrofuran / 0.25 h / 0 °C

3.1: tetrahydrofuran / 10 h / 20 °C

With vinyl acetate; ozone; In tetrahydrofuran; dichloromethane; 1.1: ozonolysis / 1.2: Rearrangement / 2.1: Grignard reaction / 3.1: Acylation;

Reference yield:

: 24190-33-8
(+)-(S)-dihydro-γ-ionone

: 308258-36-8
Propionic acid 1-[2-((S)-2,2-dimethyl-6-methylene-cyclohexyl)-ethyl]-1-methyl-allyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / tetrahydrofuran / 0.25 h / 0 °C

2: tetrahydrofuran / 10 h / 20 °C

In tetrahydrofuran; 1: Grignard reaction / 2: Acylation;