(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

Base Information

Chemical Name:(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol
CAS No.:210534-67-1
Molecular Formula:C₃₃H₃₄O₆
Molecular Weight:526.629
Hs Code.:

Synonyms:(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

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Chemical Property of (2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

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Technology Process of (2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

There total 6 articles about (2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-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: 95.0%

: 849943-91-5
phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside

: 210534-67-1
(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

Guidance literature:: With sodium methylate; In methanol; at 20 ℃; for 8h;
DOI:10.1021/jo0478609

Reference yield:

: 32860-96-1
3,4,6-tri-O-benzyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside

: 210534-67-1
(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / (+/-)-camphosulfonic acid / CH₂Cl₂ / 14 h / Heating

2: 95 percent / NaOMe / methanol / 8 h / 20 °C

With (+/-)-camphosulfonic acid; sodium methylate; In methanol; dichloromethane;
DOI:10.1021/jo0478609

Reference yield:

: 100-39-0
benzyl bromide

: 210534-67-1
(2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenoxy-tetrahydro-pyran-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: NaH; TBAI / dimethylformamide / 0.5 h

2: 57 percent / (+/-)-camphosulfonic acid / CH₂Cl₂ / 14 h / Heating

3: 95 percent / NaOMe / methanol / 8 h / 20 °C

With (+/-)-camphosulfonic acid; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium hydride; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0478609