phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside
CAS No.:189144-56-7
Molecular Formula:C₃₀H₃₂O₆S
Molecular Weight:520.646
Hs Code.:

Synonyms:phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

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Chemical Property of phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

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Technology Process of phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

There total 6 articles about phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside 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: 96.0%

: 106-95-6
allyl bromide

: 189144-55-6
phenyl 3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

: 189144-56-7
phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 23 ℃; for 1h;
DOI:10.1021/jo962300y

Reference yield:

: 2186-92-7
p-Anisaldehyde dimethyl acetal

: 189144-56-7
phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / camphorsulfonic acid / dimethylformamide / 2 h / 23 °C

2: 96 percent / NaH / dimethylformamide / 1 h / 23 °C

With camphor-10-sulfonic acid; sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1021/jo962300y

Reference yield:

: 108-98-5
thiophenol

: 189144-56-7
phenyl 2-O-allyl-3-O-benzyl-4,6-O-(4-methoxybenzylidene)-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / BF₃*Et₂O / CH₂Cl₂ / 0.5 h / 0 °C

2: 95 percent / NaOMe / methanol / 24 h / 23 °C

3: 96 percent / camphorsulfonic acid / dimethylformamide / 2 h / 23 °C

4: 96 percent / NaH / dimethylformamide / 1 h / 23 °C

With camphor-10-sulfonic acid; boron trifluoride diethyl etherate; sodium methylate; sodium hydride; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo962300y