phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside
CAS No.:692740-54-8
Molecular Formula:C₃₄H₃₄O₆S
Molecular Weight:570.706
Hs Code.:

Synonyms:phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

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Chemical Property of phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

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Technology Process of phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

There total 5 articles about phenyl 2,3-di-O-benzyl-4,6-O-p-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: 83.0%

: 100-39-0
benzyl bromide

: 225241-34-9
phenyl 4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

: 692740-54-8
phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 4h; Inert atmosphere;
DOI:10.1021/jo500449h

Reference yield:

: 2936-70-1,5624-48-6,13992-15-9,16758-34-2,28244-97-5,77481-62-0,77481-63-1,105088-17-3,149495-84-1
(2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol

: 692740-54-8
phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / camphor sulfonic acid / tetrahydrofuran / 12 h / 85 °C

2: 82 percent / NaH / dimethylformamide / 48 h / 20 °C

With camphor-10-sulfonic acid; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo035789l

Reference yield:

: 108-98-5
thiophenol

: 692740-54-8
phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 83 percent / BF₃*Et₂O / CH₂Cl₂ / 3 h / 20 °C

2: 99 percent / NaOMe / methanol; CH₂Cl₂ / 1 h / 0 °C

3: 85 percent / camphor sulfonic acid / tetrahydrofuran / 12 h / 85 °C

4: 82 percent / NaH / dimethylformamide / 48 h / 20 °C

With camphor-10-sulfonic acid; boron trifluoride diethyl etherate; sodium methylate; sodium hydride; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo035789l