(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

Base Information

Chemical Name:(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate
CAS No.:1402931-60-5
Molecular Formula:C₃₂H₃₅NO₁₀
Molecular Weight:593.631
Hs Code.:

(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

Synonyms:(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

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Chemical Property of (1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

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Technology Process of (1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

There total 17 articles about (1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate 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:

: 960365-65-5
(1R,2R,3S,3aR,8bS)-methyl 1,6,8b-trihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]-cyclopenta[d]furan-2-carboxylate

: 1402931-60-5
(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine / toluene / 0.17 h / 0 °C / Inert atmosphere; Molecular sieve

1.2: 6 h / 0 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; hydrogen / methanol / 760.05 Torr / Inert atmosphere

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

With palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; triphenylphosphine; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/jm3011542

Reference yield:

: C₃₈H₄₉NO₁₀Si

: 1402931-60-5
(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jm3011542

Reference yield:

: [2-[4-benzyloxy-2-methoxy-6-(4-methoxybenzoyl)oxyphenyl]-2-oxoethyl] 4-methoxybenzoate

: 1402931-60-5
(1R,2R,3S,3aR,8bS)-methyl 1,8b-dihydroxy-6-((2S,6R)-6-(hydroxymethyl)morpholin-2-yloxy)-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]-furan-2-carboxylate

Guidance literature:: Multi-step reaction with 9 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 2 h / -70 - -20 °C / Inert atmosphere

2.1: sulfuric acid; acetic acid / 20 h / 20 °C / Inert atmosphere

3.1: water; sodium hydroxide / ethanol / 1 h / 80 °C / Inert atmosphere

4.1: methanol; dichloromethane; acetonitrile / 10 h / 0 - 5 °C / Inert atmosphere; UV-irradiation

4.2: 1 h / 60 °C / Inert atmosphere

4.3: 48 h / Inert atmosphere

5.1: 5%-palladium/activated carbon; hydrogen / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

6.1: ChiralPak AD-H / ethanol / Inert atmosphere; Supercritical conditions; Resolution of racemate

7.1: triphenylphosphine / toluene / 0.17 h / 0 °C / Inert atmosphere; Molecular sieve

7.2: 6 h / 0 °C / Inert atmosphere

8.1: palladium 10% on activated carbon; hydrogen / methanol / 760.05 Torr / Inert atmosphere

9.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

With sulfuric acid; 5%-palladium/activated carbon; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; water; hydrogen; acetic acid; triphenylphosphine; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; acetonitrile; 1.1: |Baker-Venkataraman Rearrangement;
DOI:10.1021/jm3011542