acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

Base Information

Chemical Name:acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester
CAS No.:913193-79-0
Molecular Formula:C₂₃H₃₄O₄
Molecular Weight:374.521
Hs Code.:

Synonyms:acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

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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 acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

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Technology Process of acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

There total 18 articles about acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl 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: 77.0%

: 913193-95-0
(3S,6S)-6-((E)-(R)-2-Benzyloxy-6-methyl-hept-3-enyl)-3-methyl-tetrahydro-pyran-2-ol

: 108-24-7
acetic anhydride

: 913193-79-0
acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/jo0610412

Reference yield:

: 66688-51-5
1,1-diiodo-3-methylbutane

: 913193-79-0
acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / CrCl₂ / dimethylformamide; tetrahydrofuran / 1 h / 20 °C

2: 95 percent / DIBAL-H / hexane; CH₂Cl₂ / 0.5 h / -78 °C

3: 77 percent / triethylamine; 4-(dimethylamino)pyridine / CH₂Cl₂ / 2 h / 20 °C

With chromium dichloride; dmap; diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0610412

Reference yield:

: 502160-06-7
(2R)-2-(benzyloxy)-3-[(2S,5S)-5-methyl-6-oxo-tetrahydro-2H-pyran-2-yl]propanal

: 913193-79-0
acetic acid (3S,6S)-6-((2R)-2-benzyloxy-6-methylhept-3-enyl)-3-methyltetrahydropyran-2-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / CrCl₂ / dimethylformamide; tetrahydrofuran / 1 h / 20 °C

2: 95 percent / DIBAL-H / hexane; CH₂Cl₂ / 0.5 h / -78 °C

3: 77 percent / triethylamine; 4-(dimethylamino)pyridine / CH₂Cl₂ / 2 h / 20 °C

With chromium dichloride; dmap; diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0610412