(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Base Information

Chemical Name:(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
CAS No.:25507-02-2
Molecular Formula:C₂₀H₂₃NO₁₁S
Molecular Weight:485.469
Hs Code.:

Synonyms:(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Suppliers and Price of (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

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Technology Process of (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

There total 4 articles about (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 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: 66.0%

: 13113-79-6
sodium 4-nitrobenzenethiolate

: 572-10-1,4451-35-8,4451-36-9,14227-52-2,14227-87-3,14227-88-4,14257-40-0,17081-03-7,19186-60-8,57237-01-1,65982-17-4,65982-18-5,65982-19-6,66966-08-3,144299-57-0
2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl chloride

: 25507-02-2
(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Guidance literature:: In N,N,N,N,N,N-hexamethylphosphoric triamide; 40 deg C, 6 h; r.t.;

Reference yield:

: 25878-60-8
D-galactose pentaacetate

: 25507-02-2
(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethyl methyl ether, boron trifluoride

2: 66 percent / hexamethylphosphoric acid triamide / 40 deg C, 6 h; r.t.

With Dichloromethyl methyl ether; boron trifluoride; In N,N,N,N,N,N-hexamethylphosphoric triamide;

Reference yield:

: 40591-65-9,51224-13-6,51898-28-3,57030-42-9,106818-92-2
2,3,4,6-tetra-O-acetylgalactopyranosyl-1-β-pseudothiourea hydrobromide

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 41341-55-3
(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: 25507-02-2
(2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(4-nitrophenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Guidance literature:: With potassium carbonate; In water; acetone; for 4h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1055/s-1994-25704