(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

Base Information

Chemical Name:(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one
CAS No.:770714-52-8
Molecular Formula:C₃₁H₄₈O₅
Molecular Weight:500.719
Hs Code.:

Synonyms:(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

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Chemical Property of (1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

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Technology Process of (1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

There total 10 articles about (1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one 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: 91.0%

: 770714-51-7
(1R,3aR,4S,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-ol

: 770714-52-8
(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

Guidance literature:: With dipyridinium dichromate; Celite; In dichloromethane; for 2.5h;
DOI:10.1021/jm049340b

Reference yield:

: 770714-57-3
(1R,3aR,4S,7aR)-1-((R)-1-benzenesulfonylmethyl-5-methyl-5-trimethylsilanyloxyhexyl)-4-(tert-butyldimethylsilanyloxy)-7a-methyloctahydroindene

: 770714-52-8
(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

Guidance literature:: Multi-step reaction with 6 steps

1: BuLi / tetrahydrofuran; hexane / 5.67 h / -20 - 0 °C

2: oxalic acid dihydrate / methanol / 0.25 h

3: 0.244 g / sodium amalgam; MeOH / tetrahydrofuran / 24 h

4: 79 percent / aq. fluorosilic acid / acetonitrile / 2.5 h

5: 100 percent / pyridinium tosylate / CH₂Cl₂ / 5.75 h

6: 91 percent / pyridinium dichromate; Celite / CH₂Cl₂ / 2.5 h

With methanol; sodium amalgam; dipyridinium dichromate; n-butyllithium; Celite; fluorosilic acid; pyridinium p-toluenesulfonate; oxalic acid; In tetrahydrofuran; methanol; hexane; dichloromethane; acetonitrile;
DOI:10.1021/jm049340b

Reference yield:

: 713521-95-0
(R)-6-[(1R,3aR,4S,7aR)-4-(tert-butyldimethylsilanyloxy)-7a-methyloctahydroinden-1-yl]-7-iodo-2-methylheptan-2-ol

: 770714-52-8
(1R,3aR,7aR)-1-((S)-5-hydroxy-1-{2-[(R)-2-(4-methoxyphenyl)-5,5-dimethyl-[1,3]dioxan-4-yl]ethyl}-5-methylhexyl)-7a-methyloctahydroinden-4-one

Guidance literature:: Multi-step reaction with 8 steps

1: dimethylformamide / 3 h / Heating

2: 0.157 g / cyclohexane / 17 h

3: BuLi / tetrahydrofuran; hexane / 5.67 h / -20 - 0 °C

4: oxalic acid dihydrate / methanol / 0.25 h

5: 0.244 g / sodium amalgam; MeOH / tetrahydrofuran / 24 h

6: 79 percent / aq. fluorosilic acid / acetonitrile / 2.5 h

7: 100 percent / pyridinium tosylate / CH₂Cl₂ / 5.75 h

8: 91 percent / pyridinium dichromate; Celite / CH₂Cl₂ / 2.5 h

With methanol; sodium amalgam; dipyridinium dichromate; n-butyllithium; Celite; fluorosilic acid; pyridinium p-toluenesulfonate; oxalic acid; In tetrahydrofuran; methanol; hexane; dichloromethane; cyclohexane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm049340b