(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

Base Information

Chemical Name:(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol
CAS No.:204070-68-8
Molecular Formula:C₅₃H₇₄O₈
Molecular Weight:839.166
Hs Code.:

Synonyms:(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

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Chemical Property of (S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

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Technology Process of (S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

There total 4 articles about (S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-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:

: 204070-51-9
(3R,4S,5R,6R)-2-((R)-1-Allyloxymethyl-2-hexadecyloxy-ethoxy)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran

: 204070-68-8
(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

Guidance literature:: With water; toluene-4-sulfonic acid; palladium on activated charcoal; In methanol; isopropyl alcohol; at 80 ℃; Yield given;
DOI:10.1002/(SICI)1521-3773(19980216)37:3<351::AID-ANIE351>3.0.CO;2-P

Reference yield:

: 78153-79-4
2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl fluoride

: 204070-68-8
(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / AgClO₄, SnCl₂, molecular sieves 4 Angstroem / diethyl ether / -15 °C

2: 91 percent / KOH / methanol

3: NaH / tetrahydrofuran / 80 °C

4: p-toluenesulfonic acid, H₂O / Pd/C / methanol; propan-2-ol / 80 °C

With potassium hydroxide; 4 A molecular sieve; water; silver perchlorate; sodium hydride; toluene-4-sulfonic acid; tin(ll) chloride; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; isopropyl alcohol;
DOI:10.1002/(SICI)1521-3773(19980216)37:3<351::AID-ANIE351>3.0.CO;2-P

Reference yield:

: 204070-40-6
(R)-3-Allyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

: 204070-68-8
(S)-3-Hexadecyloxy-2-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-propan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / tetrahydrofuran / 80 °C

2: p-toluenesulfonic acid, H₂O / Pd/C / methanol; propan-2-ol / 80 °C

With water; sodium hydride; toluene-4-sulfonic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; isopropyl alcohol;
DOI:10.1002/(SICI)1521-3773(19980216)37:3<351::AID-ANIE351>3.0.CO;2-P