5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

Base Information

Chemical Name:5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose
CAS No.:162517-93-3
Molecular Formula:C₂₇H₃₈O₇SSi
Molecular Weight:534.746
Hs Code.:

Synonyms:5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

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Chemical Property of 5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

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Technology Process of 5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

There total 9 articles about 5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose 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: 98.0%

: 162517-92-2
5-O-(tert-butyldiphenylsilyl)-3-C-(2'-hydroxyethyl)-3-deoxy-1,2-O-isopropylidene-β-D-lyxofuranose

: 124-63-0
methanesulfonyl chloride

: 162517-93-3
5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

Guidance literature:: In pyridine; at 0 ℃; for 3h;
DOI:10.1016/0040-4020(94)01009-O

Reference yield:

: 172751-32-5
5-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-β-D-threo-pentofuranose-3-ulose

: 162517-93-3
5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

Guidance literature:: Multi-step reaction with 4 steps

1: benzene / 4 h / Heating

2: H₂ / 10percent Pd/C / ethyl acetate / 48 h / Ambient temperature

3: 88 percent / LiAlH₄ / tetrahydrofuran / 1 h / Ambient temperature

4: 98 percent / pyridine / 3 h / 0 °C

With lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; pyridine; ethyl acetate; benzene;
DOI:10.1016/0040-4020(94)01009-O

Reference yield:

: 114738-04-4
(3aS,5R,6R,6aS)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol

: 162517-93-3
5-O-(tert-butyldiphenylsilyl)-3-C-(2'-O-methanesulfonyl-2'-hydroxyethyl)-3-deoxy-1,2-isopropylidene-β-D-lyxofuranose

Guidance literature:: Multi-step reaction with 5 steps

1: pyridinium perchlorate, 3A molecular sieve / CH₂Cl₂ / 4 h / Ambient temperature

2: benzene / 4 h / Heating

3: H₂ / 10percent Pd/C / ethyl acetate / 48 h / Ambient temperature

4: 88 percent / LiAlH₄ / tetrahydrofuran / 1 h / Ambient temperature

5: 98 percent / pyridine / 3 h / 0 °C

With lithium aluminium tetrahydride; 3 A molecular sieve; hydrogen; pyridinium perchlorate; palladium on activated charcoal; In tetrahydrofuran; pyridine; dichloromethane; ethyl acetate; benzene;
DOI:10.1016/0040-4020(94)01009-O