(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

Base Information

Chemical Name:(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane
CAS No.:260364-27-0
Molecular Formula:C₂₃H₃₆O₈SSi
Molecular Weight:500.686
Hs Code.:

Synonyms:(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

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Chemical Property of (4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

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Technology Process of (4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

There total 8 articles about (4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane 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: 54.0%

: 260364-26-9
(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-9-O-(trimethylsilyl)-1,6-dioxaspiro[4.5]decane

: 260364-27-0
(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

Guidance literature:: With potassium carbonate; In methanol; at 0 ℃; for 4h;
DOI:10.1016/s0040-4020(99)00990-4

Reference yield:

: 85272-31-7
di-tert-butylsilyl bis(trifluoromethanesulfonate)

: 260364-27-0
(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / 2,6-lutidine / CH₂Cl₂; dimethylformamide / 0 - 20 °C

2: 99 percent / imidazole / tetrahydrofuran / 0 - 20 °C

3: 40 percent / n-BuLi / tetrahydrofuran; hexane / -78 - 20 °C

4: 94 percent / NaBH₄ / methanol / 3 h / 0 - 20 °C

5: 54 percent / K₂CO₃ / methanol / 4 h / 0 °C

With 1H-imidazole; 2,6-dimethylpyridine; sodium tetrahydroborate; n-butyllithium; potassium carbonate; In tetrahydrofuran; methanol; hexane; dichloromethane; N,N-dimethyl-formamide; 1: Etherification / 2: silylation / 3: Addition / 4: Reduction / 5: desilylation;
DOI:10.1016/s0040-4020(99)00990-4

Reference yield:

: 130307-35-6
3-(phenylthio)-4,5-dihydrofuran

: 260364-27-0
(4R,5R,7R,8R,9R,10R)-7,8-O-(di-tert-butylsilylene)-8,9,10-trihydroxy-7-hydroxymethyl-4-phenylsulfonyl-1,6-dioxaspiro[4.5]decane

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / MCPBA / CH₂Cl₂ / 0.5 h / 0 °C

2: 40 percent / n-BuLi / tetrahydrofuran; hexane / -78 - 20 °C

3: 94 percent / NaBH₄ / methanol / 3 h / 0 - 20 °C

4: 54 percent / K₂CO₃ / methanol / 4 h / 0 °C

With sodium tetrahydroborate; n-butyllithium; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; hexane; dichloromethane; 1: Oxidation / 2: Addition / 3: Reduction / 4: desilylation;
DOI:10.1016/s0040-4020(99)00990-4