Technology Process of 6-[(2S,3R,4S,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoic acid methyl ester
There total 4 articles about 6-[(2S,3R,4S,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoic acid methyl ester which
guide to synthetic route it.
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synthetic route:
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189144-69-2
6-[(2S,3R,4S,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoic acid methyl ester
- Guidance literature:
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Multi-step reaction with 3 steps
1: 80 percent / hex-1-ene, ethyldiisopropylamine / CH2Cl2 / 36 h / 23 °C
2: 83 percent / H2, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr
3: 1.) Ag2CO3, 4 Angstroem molecular sieves, 2.) AgClO4 / 1) CH2Cl2, 23 deg C, 1 h; 2) CH2Cl2, 0 deg C, 80 min
With
1-hexene; 4 A molecular sieve; hydrogen; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate;
palladium on activated charcoal;
In
ethanol; dichloromethane;
DOI:10.1021/jo962300y
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189144-69-2
6-[(2S,3R,4S,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoic acid methyl ester
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 80 percent / hex-1-ene, ethyldiisopropylamine / CH2Cl2 / 36 h / 23 °C
2: 83 percent / H2, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr
3: 1.) Ag2CO3, 4 Angstroem molecular sieves, 2.) AgClO4 / 1) CH2Cl2, 23 deg C, 1 h; 2) CH2Cl2, 0 deg C, 80 min
With
1-hexene; 4 A molecular sieve; hydrogen; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate;
palladium on activated charcoal;
In
ethanol; dichloromethane;
DOI:10.1021/jo962300y
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-
189144-69-2
6-[(2S,3R,4S,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexanoic acid methyl ester
- Guidance literature:
-
Multi-step reaction with 4 steps
1: bromine / CH2Cl2 / 0.08 h / 0 - 23 °C
2: 80 percent / hex-1-ene, ethyldiisopropylamine / CH2Cl2 / 36 h / 23 °C
3: 83 percent / H2, AcOH / Pd-C / ethanol / 24 h / 23 °C / 10343 Torr
4: 1.) Ag2CO3, 4 Angstroem molecular sieves, 2.) AgClO4 / 1) CH2Cl2, 23 deg C, 1 h; 2) CH2Cl2, 0 deg C, 80 min
With
1-hexene; 4 A molecular sieve; hydrogen; bromine; silver perchlorate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate;
palladium on activated charcoal;
In
ethanol; dichloromethane;
DOI:10.1021/jo962300y