Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester
CAS No.:213767-10-3
Molecular Formula:C₃₅H₄₄O₇Si
Molecular Weight:604.816
Hs Code.:

Synonyms:Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

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Chemical Property of Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

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Technology Process of Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

There total 7 articles about Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester 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: 84.0%

: 108-24-7
acetic anhydride

: 213767-05-6
(2S,3S,4R,5R,6R)-4-Allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-ol

: 213767-10-3
Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

Guidance literature:: In pyridine; Ambient temperature;
DOI:10.1021/jo9806097

Reference yield:

: 100-39-0
benzyl bromide

: 213767-10-3
Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / NaH / dimethylformamide / 1.) 0 deg C, 30 min, 2.) o deg C to room temperature

2: 84 percent / 80percent AcOH / 4 h / 80 °C

3: 1.) dibutyltin oxide, 2.) tetrabutylammonium iodide / 1.) MeOH, reflux, 2.5 h, 2.) toluene, 60 deg C, 15 h

4: 84 percent / pyridine / Ambient temperature

With tetra-(n-butyl)ammonium iodide; sodium hydride; di(n-butyl)tin oxide; acetic acid; In pyridine; N,N-dimethyl-formamide;
DOI:10.1021/jo9806097

Reference yield:

: 131089-35-5
methyl 6-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-α-D-mannopyranoside

: 213767-10-3
Acetic acid (2S,3S,4S,5R,6R)-4-allyloxy-5-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / NaH / dimethylformamide / 1.) 0 deg C, 30 min, 2.) o deg C to room temperature

2: 84 percent / 80percent AcOH / 4 h / 80 °C

3: 1.) dibutyltin oxide, 2.) tetrabutylammonium iodide / 1.) MeOH, reflux, 2.5 h, 2.) toluene, 60 deg C, 15 h

4: 84 percent / pyridine / Ambient temperature

With tetra-(n-butyl)ammonium iodide; sodium hydride; di(n-butyl)tin oxide; acetic acid; In pyridine; N,N-dimethyl-formamide;
DOI:10.1021/jo9806097