2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

Base Information

Chemical Name:2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate
CAS No.:944450-13-9
Molecular Formula:C₁₉H₃₂O₄
Molecular Weight:324.461
Hs Code.:

Synonyms:2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

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Chemical Property of 2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

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Technology Process of 2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

There total 5 articles about 2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate 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: 96.0%

: 944450-10-6
2-[(1S,2R,6R)-2-hydroxy-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

: 107-30-2
chloromethyl methyl ether

: 944450-13-9
2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jo070165r

Reference yield:

: 944450-08-2
ethyl 2-[(1S,6R)-4-methyl-2-oxo-6-(prop-1-en-2-yl)cyclohex-3-enyl]acetate

: 944450-13-9
2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / lithium aluminum hydride / diethyl ether / -78 - 20 °C

2: 78 percent / pyridine / 0.5 h / 0 °C

3: 96 percent / ethyldiisopropylamine / CH₂Cl₂ / 0 - 20 °C

With pyridine; lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane;
DOI:10.1021/jo070165r

Reference yield:

: 944450-09-3
(1R,5R,6S)-6-(2-hydroxyethyl)-3-methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

: 944450-13-9
2-[(1S,2R,6R)-2-(methoxymethoxy)-4-methyl-6-(prop-1-en-2-yl)cyclohex-3-enyl]ethyl pivalate

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridine / 0.5 h / 0 °C

2: 96 percent / ethyldiisopropylamine / CH₂Cl₂ / 0 - 20 °C

With pyridine; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo070165r