Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester
CAS No.:90670-44-3
Molecular Formula:C₂₈H₃₀O₆S
Molecular Weight:494.609
Hs Code.:

Synonyms:Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

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Chemical Property of Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

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Technology Process of Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

There total 9 articles about Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-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: 98.0%

: 90670-43-2
Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

: 90670-44-3
Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 25 ℃;
DOI:10.1021/ja00327a021

Reference yield:

: 13992-16-0
Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester

: 90670-44-3
Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1: NaOMe / methanol / 0 - 25 °C

2: CSA / benzene / 25 °C

3: NaH / tetrahydrofuran / 25 - 60 °C

4: amberlyst 15 / methanol / Heating

5: imid / dimethylformamide / 0 - 25 °C

6: DMAP / CH₂Cl₂ / 0 - 25 °C

7: 98 percent / n-Bu₄NF / tetrahydrofuran / 0 - 25 °C

With 1H-imidazole; dmap; Amberlyst 15; tetrabutyl ammonium fluoride; sodium methylate; sodium hydride; camphor-10-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ja00327a021

Reference yield:

: 13992-15-9
phenyl-1-thio-α-D-glucopyranoside

: 90670-44-3
Acetic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 6 steps

1: CSA / benzene / 25 °C

2: NaH / tetrahydrofuran / 25 - 60 °C

3: amberlyst 15 / methanol / Heating

4: imid / dimethylformamide / 0 - 25 °C

5: DMAP / CH₂Cl₂ / 0 - 25 °C

6: 98 percent / n-Bu₄NF / tetrahydrofuran / 0 - 25 °C

With 1H-imidazole; dmap; Amberlyst 15; tetrabutyl ammonium fluoride; sodium hydride; camphor-10-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ja00327a021