Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

Base Information

Chemical Name:Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate
CAS No.:223907-24-2
Molecular Formula:C₂₃H₃₂O₄
Molecular Weight:372.505
Hs Code.:

Synonyms:Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

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Chemical Property of Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

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Technology Process of Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

There total 6 articles about Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate 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: 54.0%

: 223907-23-1
Methyl (2Z,6E)-7-methyl-9-[(2S,3S)-3-methyl-3-(benzyloxymethyl)oxiran-2-yl]-3-[(trimethylsilyl)methyl]nona-2,6-dienoate

: 223907-24-2
Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.166667h;
DOI:10.1039/a906589j

Reference yield:

: 116179-52-3
(-)-6,7-epoxy-8-(benzyloxy)geranyl alcohol

: 223907-24-2
Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: NEt₃; MeSO₂Cl / tetrahydrofuran / 1 h / -78 °C

1.2: 79 percent / LiBr / tetrahydrofuran; acetone / 0.67 h / -78 °C

2.1: NaH; n-BuLi / tetrahydrofuran; hexane / 0.33 h / 0 °C

2.2: 78 percent / tetrahydrofuran; hexane / 17 h / 20 °C

3.1: NaH / diethyl ether / 0.33 h / 0 °C

3.2: 93 percent / diethyl ether / 2.5 h / 20 °C

4.1: 54 percent / nickel(II) acetylacetonate / diethyl ether / 0.17 h / 0 °C

5.1: 54 percent / BF₃*OEt₂ / CH₂Cl₂ / 0.17 h / 20 °C

With bis(acetylacetonate)nickel(II); n-butyllithium; boron trifluoride diethyl etherate; sodium hydride; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; 1.1: Mesylation / 1.2: Substitution / 2.1: Metallation / 2.2: Alkylation / 3.1: Metallation / 3.2: Esterification / 4.1: Alkylation / 5.1: Cyclization;
DOI:10.1039/a906589j

Reference yield:

: 223907-19-5
(2S,3S)-3-[(E)-5-bromo-3-methylpent-3-enyl]-2-methyl-2-(benzyloxymethyl)oxirane

: 223907-24-2
Methyl (4aS,5R,6S,8aS)-6-hydroxy-5,8a-dimethyl-2-methylene-5-(benzyloxymethyl)perhydronaphthalene-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH; n-BuLi / tetrahydrofuran; hexane / 0.33 h / 0 °C

1.2: 78 percent / tetrahydrofuran; hexane / 17 h / 20 °C

2.1: NaH / diethyl ether / 0.33 h / 0 °C

2.2: 93 percent / diethyl ether / 2.5 h / 20 °C

3.1: 54 percent / nickel(II) acetylacetonate / diethyl ether / 0.17 h / 0 °C

4.1: 54 percent / BF₃*OEt₂ / CH₂Cl₂ / 0.17 h / 20 °C

With bis(acetylacetonate)nickel(II); n-butyllithium; boron trifluoride diethyl etherate; sodium hydride; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; 1.1: Metallation / 1.2: Alkylation / 2.1: Metallation / 2.2: Esterification / 3.1: Alkylation / 4.1: Cyclization;
DOI:10.1039/a906589j