(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

Base Information

Chemical Name:(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol
CAS No.:313944-60-4
Molecular Formula:C₃₃H₄₈O₇Si
Molecular Weight:584.825
Hs Code.:

Synonyms:(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

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Chemical Property of (1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

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Technology Process of (1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

There total 6 articles about (1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol 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: 74.0%

: 313944-59-1
(1S,2R,3S,4S,5R,8S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-1,8-bis-methoxymethoxy-2-methyl-3-(2-oxo-ethyl)-bicyclo[2.2.2]octane-2-carbaldehyde

: 313944-60-4
(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

Guidance literature:: With samarium diiodide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; at 20 ℃;
DOI:10.1016/S0040-4039(00)01413-1

Reference yield:

: 313944-68-2
2-[(1S,2S,3S,4S,6R,7S)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-4,7-bis-methoxymethoxy-3-methyl-bicyclo[2.2.2]oct-2-yl]-ethanol

: 313944-60-4
(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / PCC

2: 74 percent / SmI₂ / tetrahydrofuran; hexamethylphosphoric acid triamide / 20 °C

With samarium diiodide; pyridinium chlorochromate; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 1: Oxidation / 2: Cyclization;
DOI:10.1016/S0040-4039(00)01413-1

Reference yield:

: 313944-58-0
(1S,2R,3S,4S,5R)-3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(tert-butyl-diphenyl-silanyloxymethyl)-1-methoxymethoxy-2-methyl-8-oxo-bicyclo[2.2.2]octane-2-carboxylic acid methyl ester

: 313944-60-4
(1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol

Guidance literature:: Multi-step reaction with 6 steps

1: 73 percent / NaBH₄

2: 100 percent / iPr₂NEt

3: 96 percent / LiAlH₄

4: 96 percent / PPTS / methanol

5: 62 percent / PCC

6: 74 percent / SmI₂ / tetrahydrofuran; hexamethylphosphoric acid triamide / 20 °C

With sodium tetrahydroborate; lithium aluminium tetrahydride; samarium diiodide; pyridinium p-toluenesulfonate; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; 1: Reduction / 2: Etherification / 3: Reduction / 4: Substitution / 5: Oxidation / 6: Cyclization;
DOI:10.1016/S0040-4039(00)01413-1