(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

Base Information

Chemical Name:(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol
CAS No.:392235-17-5
Molecular Formula:C₂₃H₃₈O₃Si
Molecular Weight:390.638
Hs Code.:

Synonyms:(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

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Chemical Property of (1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

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Technology Process of (1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

There total 5 articles about (1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol 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: 53.0%

: 392235-13-1
(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a,5-diol

: 392235-17-5
(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

Guidance literature:: With Ranye-Ni; In ethanol; for 8h; Heating;
DOI:10.1021/jm011001k

Reference yield:

: 33879-04-8,51065-67-9
(+)-(3aS,7aS)-2,3,3a,4,7,7a-hexahydro-3a-hydroxy-7a-methyl-1H-indene-1,5(6H)-dione

: 392235-17-5
(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 83 percent / oxalic acid / acetonitrile / 16 h

2.1: 77 percent / t-BuOK / 2-methyl-propan-2-ol; tetrahydrofuran / 2 h / Heating

3.1: BH₃ / tetrahydrofuran / 1 h / 20 °C

3.2: 20 percent / NaBO₃; aq. NaOH / 16 h / 20 °C

4.1: 68 percent / 1 N pTSA / acetonitrile; H₂O / 16 h

5.1: n-butyllithium / hexane / 4 h / 20 °C

5.2: 43 percent / hexane; tetrahydrofuran / 1.5 h / -78 °C

6.1: 53 percent / Ranye-Ni / ethanol / 8 h / Heating

With n-butyllithium; Ranye-Ni; borane; potassium tert-butylate; oxalic acid; toluene-4-sulfonic acid; In tetrahydrofuran; ethanol; hexane; water; acetonitrile; tert-butyl alcohol; 2.1: Wittig reaction;
DOI:10.1021/jm011001k

Reference yield:

: 178379-39-0
(1S,3aS,7aR)-1-hydroxymethyl-3a-hydroxy-7a-methyl-5-perhydroindenone

: 392235-17-5
(1S,3aS,5S,7aR)-1-hydroxymethyl-5-(4-tert-butyldimethylsilyloxyphenyl)-7a-methylperhydroinden-3a-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / hexane / 4 h / 20 °C

1.2: 43 percent / hexane; tetrahydrofuran / 1.5 h / -78 °C

2.1: 53 percent / Ranye-Ni / ethanol / 8 h / Heating

With n-butyllithium; Ranye-Ni; In ethanol; hexane;
DOI:10.1021/jm011001k