(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

Base Information

Chemical Name:(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one
CAS No.:215033-23-1
Molecular Formula:C₂₉H₃₃NO₆
Molecular Weight:491.584
Hs Code.:

Synonyms:(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

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Chemical Property of (Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

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Technology Process of (Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

There total 2 articles about (Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one 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: 85.0%

: 103-71-9
phenyl isocyanate

: 162992-65-6
(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-hydroxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

: 215033-23-1
(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

Guidance literature:: With triethylamine; In dichloromethane; Ambient temperature;
DOI:10.1039/a804276d

Reference yield:

: (1S,5R,6R,7R,1'RS)-7-Benzoyloxy-6-(1'-hydroxyoct-2'-ynyl)-2-oxabicyclo[3.3.0]octan-3-one

: 215033-23-1
(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / H₂, quinoline / Pd, MnCl₂ / methanol / Ambient temperature

2: 85 percent / Et₃N / CH₂Cl₂ / Ambient temperature

With quinoline; hydrogen; triethylamine; palladium; manganese(ll) chloride; In methanol; dichloromethane;
DOI:10.1039/a804276d

Reference yield:

: 215033-23-1
(Z)-(1S,5R,6R,7R,1'S)-7-Benzoyloxy-6-(1'-N-phenylcarbamoyloxyoct-2'-enyl)-2-oxabicyclo[3.3.0]octan-3-one

: 51705-58-9
[3aR,4R(1E,3R),5R,6aS]-5-benzoyloxy-4-(3-hydroxyocten-1-yl)-hexahydro-2H-cyclopenta[b]furan-2-one

Guidance literature:: Multi-step reaction with 3 steps

2: BF₃*2AcOH / CH₂Cl₂ / 0.08 h / -10 °C

3: H₂O₂, KF, H₂O / tetrahydrofuran; methanol / 2 h / Heating

With potassium fluoride; water; dihydrogen peroxide; boron trifluoride diacetate; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1039/a804276d