(2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

Base Information

Chemical Name:(2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane
CAS No.:162490-79-1
Molecular Formula:C₂₈H₄₂O₆Si
Molecular Weight:502.723
Hs Code.:

Synonyms:

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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 (2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

Chemical Property:

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Technology Process of (2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

There total 6 articles about (2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane 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:

: 125975-53-3,147220-48-2,116996-54-4
(2S)-O-(tert-butyldiphenylsilyl)-1,2-epoxybutan-4-ol

: 162490-79-1
(2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) n-BuLi / 1.) THF, hexane, -30 deg C, 2 h, 2.) THF, hexane, -20 deg C, 28 h

2: 80 percent / CaCO₃, MeI / acetonitrile; H₂O / 24 h / Ambient temperature

3: 88 percent / LiI, LiAlH(O^tBu)3 / diethyl ether / 0.75 h / 0 °C

4: 82 percent / iso-Pr₂NEt / CH₂Cl₂ / 16 h

5: 84 percent / pyridinium p-toluenesulfonate / methanol / 3.5 h / 40 °C

6: 1.) t-BuCOCl, pyridine, 2.) CH₃SO₂Cl, Et₃N, 3.) KH

With pyridine; n-butyllithium; pyridinium p-toluenesulfonate; pivaloyl chloride; potassium hydride; methanesulfonyl chloride; lithium tri-t-butoxyaluminum hydride; triethylamine; N-ethyl-N,N-diisopropylamine; calcium carbonate; lithium iodide; methyl iodide; In methanol; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1248/cpb.42.2161

Reference yield:

: 162490-78-0
(2R,4R,6S)-8-(tert-butyldiphenylsiloxy)-1,2-(isopropylidenedioxy)octan-4,6-diol

: 162490-79-1
(2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / iso-Pr₂NEt / CH₂Cl₂ / 16 h

2: 84 percent / pyridinium p-toluenesulfonate / methanol / 3.5 h / 40 °C

3: 1.) t-BuCOCl, pyridine, 2.) CH₃SO₂Cl, Et₃N, 3.) KH

With pyridine; pyridinium p-toluenesulfonate; pivaloyl chloride; potassium hydride; methanesulfonyl chloride; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1248/cpb.42.2161

Reference yield:

: 162409-79-2
(2R,6S)-8-(tert-butyldiphenylsiloxy)-1,2-(isopropylidenedioxy)octan-4-one-6-ol

: 162490-79-1
(2S,4R,6S)-8-(tert-butyldiphenylsiloxy)-4,6-bis(methoxymethoxy)-1,2-epoxyoctane

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / LiI, LiAlH(O^tBu)3 / diethyl ether / 0.75 h / 0 °C

2: 82 percent / iso-Pr₂NEt / CH₂Cl₂ / 16 h

3: 84 percent / pyridinium p-toluenesulfonate / methanol / 3.5 h / 40 °C

4: 1.) t-BuCOCl, pyridine, 2.) CH₃SO₂Cl, Et₃N, 3.) KH

With pyridine; pyridinium p-toluenesulfonate; pivaloyl chloride; potassium hydride; methanesulfonyl chloride; lithium tri-t-butoxyaluminum hydride; triethylamine; N-ethyl-N,N-diisopropylamine; lithium iodide; In methanol; diethyl ether; dichloromethane;
DOI:10.1248/cpb.42.2161