((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

Base Information

Chemical Name:((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol
CAS No.:652153-23-6
Molecular Formula:C₁₉H₂₆O₂
Molecular Weight:286.414
Hs Code.:

Synonyms:((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

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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 ((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

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Technology Process of ((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

There total 3 articles about ((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol 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: 86.0%

: 652153-16-7
(4aR,6R,8aS)-3,4,4a,5,6,7,8,8a-octahydro-8a-methyl-6-(phenylmethoxy)naphthalen-1-carboxylic acid methyl ester

: 652153-23-6
((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; at -78 ℃;
DOI:10.1002/hlca.200390315

Reference yield:

: (4aR,6R,8aR)-6-Benzyloxy-8a-methyl-octahydro-naphthalen-1-one

: 652153-23-6
((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / Proton Sponge(R) / CH₂Cl₂ / 16 h / 20 °C

2: 83 percent / K₂CO₃; LiCl; 1-methylpyrrolidin-2-one / dichlorobis(triphenylphosphine)palladium / 24 h / 130 °C / 10343 Torr

3: 86 percent / Dibal-H / CH₂Cl₂ / -78 °C

With 1-methyl-pyrrolidin-2-one; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; diisobutylaluminium hydride; potassium carbonate; lithium chloride; bis-triphenylphosphine-palladium(II) chloride; In dichloromethane;
DOI:10.1002/hlca.200390315

Reference yield:

: 652153-15-6
(4aR,6R,8aS)-3,4,4a,5,6,7,8,8a-octahydro-8a-methyl-6-(phenylmethoxy)naphthalen-1-ol trifluoronethanesulfonate

: 652153-23-6
((4aR,6R,8aR)-6-Benzyloxy-8a-methyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / K₂CO₃; LiCl; 1-methylpyrrolidin-2-one / dichlorobis(triphenylphosphine)palladium / 24 h / 130 °C / 10343 Torr

2: 86 percent / Dibal-H / CH₂Cl₂ / -78 °C

With 1-methyl-pyrrolidin-2-one; diisobutylaluminium hydride; potassium carbonate; lithium chloride; bis-triphenylphosphine-palladium(II) chloride; In dichloromethane;
DOI:10.1002/hlca.200390315