Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

Base Information

Chemical Name:Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester
CAS No.:251547-26-9
Molecular Formula:C₅₉H₉₂O₂₃
Molecular Weight:1169.37
Hs Code.:

Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

Synonyms:Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

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Chemical Property of Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

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Technology Process of Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

There total 1 articles about Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-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: 60.0%

: 29654-55-5
5-(hydroxymethyl)benzene-1,3-diol

: 251547-27-0
Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-iodo-dodecyloxy)-tetrahydro-pyran-4-yl ester

: Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-[12-(3-hydroxy-5-hydroxymethyl-phenoxy)-dodecyloxy]-tetrahydro-pyran-4-yl ester

: 251547-26-9
Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: With 18-crown-6 ether; 4-Angstroem MS; potassium carbonate; In acetonitrile; for 8h; Heating;
DOI:10.1016/S0040-4039(99)01558-0

Reference yield: 100.0%

: 124-63-0
methanesulfonyl chloride

: 251547-26-9
Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

: Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-methanesulfonyloxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1016/S0040-4039(99)01558-0

Reference yield:

: 251547-26-9
Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-(12-{3-hydroxymethyl-5-[12-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-phenoxy}-dodecyloxy)-tetrahydro-pyran-4-yl ester

: {3,5-Bis-[12-((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-dodecyloxy]-benzyl}-trimethyl-ammonium; bromide

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

2: 92 percent / KBr / butan-2-one / 0.5 h / Heating

3: 98 percent / NaOMe / methanol / 0.5 h / 20 °C

4: 83 percent / methanol / 1.5 h / Heating

With sodium methylate; triethylamine; potassium bromide; In methanol; dichloromethane; butanone; 1: Esterification / 2: Substitution / 3: Deacetylation / 4: Menshutkin's quaternarization;
DOI:10.1016/S0040-4039(99)01558-0