(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

Base Information

Chemical Name:(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol
CAS No.:565462-96-6
Molecular Formula:C₃₄H₃₆O₅S
Molecular Weight:556.723
Hs Code.:

Synonyms:(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

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Chemical Property of (2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

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Technology Process of (2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

There total 4 articles about (2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-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: 90.0%

: 565462-94-4
tetrahydropyran-2-yl 2,3,4,6-tetra-O-benzyl-5-deoxy-5-thio-α-D-glucopyranoside

: 565462-96-6
(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

Guidance literature:: With perchloric acid; In methanol; at 20 ℃; for 3h;
DOI:10.1016/j.bmc.2005.05.028

Reference yield:

: 137886-82-9
2,3,4,6-Tetra-O-acetyl-5-thio-α-D-glucopyranose

: 565462-96-6
(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / p-TsOH / CH₂Cl₂ / 1.5 h / 0 °C

2: 82 percent / NaOMe / methanol / 3.5 h / 20 °C

3: 88 percent / NaH / dimethylformamide / 1 h / 20 °C

4: 90 percent / HClO₄ / methanol / 3 h / 20 °C

With perchloric acid; sodium methylate; sodium hydride; toluene-4-sulfonic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.05.028

Reference yield:

: 453524-96-4
tetrahydropyran-2-yl 5-deoxy-5-thio-α-D-glucopyranoside

: 565462-96-6
(2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-thiopyran-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / NaH / dimethylformamide / 1 h / 20 °C

2: 90 percent / HClO₄ / methanol / 3 h / 20 °C

With perchloric acid; sodium hydride; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.05.028