(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

Base Information

Chemical Name:(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran
CAS No.:1442018-32-7
Molecular Formula:C₃₄H₃₄O₆S
Molecular Weight:570.706
Hs Code.:

Synonyms:(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

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Chemical Property of (2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

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Technology Process of (2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

There total 5 articles about (2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran 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: 87.0%

: 1426171-76-7
(2R,3S,4R,4aS,10bS)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

: 1442018-32-7
(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 0.25h; stereoselective reaction;
DOI:10.1080/07328303.2013.789106

Reference yield:

: 1426171-70-1
(2R,3S,4R,4aS,10bS)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydrothiochromeno[4,3-b]pyran

: 1442018-32-7
(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

Guidance literature:: Multi-step reaction with 2 steps

1: Oxone; aluminum oxide / water; dichloromethane / 12 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 20 °C

With aluminum oxide; Oxone; sodium hydride; In dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1080/07328303.2013.789106

Reference yield:

: 108-98-5
thiophenol

: 1442018-32-7
(2R,3S,4R,4aS,10bR)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-2,3,4,4a,5,10b-hexahydro-S,S-dioxothiochromeno[4,3-b]pyran

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 20 °C / Inert atmosphere

1.2: 0.08 h / 20 °C / Inert atmosphere

2.1: boron trifluoride diethyl etherate / dichloromethane / 0.08 h / 0 °C / Inert atmosphere; Molecular sieve

3.1: aluminum oxide; water; Oxone / dichloromethane / 12 h / 20 °C

4.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 20 °C

With aluminum oxide; Oxone; boron trifluoride diethyl etherate; water; sodium hydride; In dichloromethane; N,N-dimethyl-formamide; mineral oil; 2.1: |Friedel-Crafts Alkylation;
DOI:10.1016/j.ejmech.2014.09.060