(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

Base Information

Chemical Name:(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol
CAS No.:135419-73-7
Molecular Formula:C₃₄H₄₂O₅SSi
Molecular Weight:590.856
Hs Code.:

Synonyms:(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

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Chemical Property of (1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

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Technology Process of (1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

There total 6 articles about (1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-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: 88.0%

: 131414-04-5
(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylthio)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

: 135419-73-7
(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

Guidance literature:: With Oxone; pH 4 aqueous buffer; In tetrahydrofuran; methanol; for 3.5h; Ambient temperature;

Reference yield: 22.0%

: 135419-72-6
(1S,4S,6S)-6-<(tert-butyldiphenylsilyloxy)methyl>-4-methyl-1-<1-methylene-3-(phenylsulphonyl)propyl>cyclohex-2-enol

: 135419-73-7
(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

: 135419-74-8
<1S,2R(R),3S,5S,6S>-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<2-<2-(phenylsulphonylethyl)>oxiran-2-yl>-7-oxabicyclo<4.1.0>heptan-2-ol

Guidance literature:: With tert.-butylhydroperoxide; vanadyl acetylacetonate; In dichloromethane; toluene; Ambient temperature; 0 deg C to RT;

Reference yield:

: 127785-52-8
2-bromo-4-phenylthiobut-1-ene

: 135419-73-7
(1S,2S,3S,5S,6S)-3-<(tert-butyldiphenylsilyloxy)methyl>-5-methyl-2-<1-methylene-3-(phenylsulphonyl)propyl>-7-oxabicyclo<4.1.0>heptan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) tert-BuLi / 1.) pentane, ether, THF, -78 deg C, 5 min, 2.) -78 deg C, 5 min

2: 89 percent / oxone, pH 4 aqueous buffer / tetrahydrofuran; methanol / 2 h / Ambient temperature

3: 69 percent / tert-butyl hydroperoxide, vanadyl acetylacetonate / toluene; CH₂Cl₂ / Ambient temperature; 0 deg C to RT

With tert.-butylhydroperoxide; Oxone; pH 4 aqueous buffer; vanadyl acetylacetonate; tert.-butyl lithium; In tetrahydrofuran; methanol; dichloromethane; toluene;