(2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

Base Information

Chemical Name:(2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate
CAS No.:669763-28-4
Molecular Formula:C₂₁H₂₄Cl₃NO₁₀
Molecular Weight:556.781
Hs Code.:

Synonyms:(2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

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Chemical Property of (2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

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Technology Process of (2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

There total 1 articles about (2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate 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: 88.0%

: 3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranosyl trichloroacetimidate

: 108-95-2,27073-41-2
phenol

: 669763-28-4
(2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at -20 ℃; for 2.5h; Molecular sieve;
DOI:10.1007/s10719-018-9839-2

Reference yield:

: 669763-28-4
(2S,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate

: 5574-80-1
phenyl 2-acetamido-2-deoxy-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid; zinc / dichloromethane; methanol / 2.5 h / 20 °C

2.1: pyridine / dichloromethane / 2.5 h / 0 - 20 °C

3.1: sodium methylate / methanol / 1.5 h / 20 °C

3.2: Amberlite IRC-50 H+ resin

With pyridine; sodium methylate; acetic acid; zinc; In methanol; dichloromethane;
DOI:10.1007/s10719-018-9839-2