(3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate → (1S,5R,6R,7R)-6-[(E)-3-Oxo-3-({2RS}-1,3-benzodioxan-2-yl)-1-propenyl]-7-benzoyloxy-2-oxabicyclo[3,3,0]octan-3-one

HRID 1856056Notes

Reaction equation

HRID 1856056 reaction equation
[CH:1]([C@H:3]1[C@H:10]([O:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][C@H:8]2[C@@H:4]1[CH2:5][C:6](=[O:20])[O:7]2)=O.[O:21]=[C:22]([CH:43]1[O:48][C:47]2[CH:49]=[CH:50][CH:51]=[CH:52][C:46]=2[CH2:45][O:44]1)[CH:23]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>C1C=CC=CC=1>[O:21]=[C:22]([CH:43]1[O:48][C:47]2[CH:49]=[CH:50][CH:51]=[CH:52][C:46]=2[CH2:45][O:44]1)/[CH:23]=[CH:1]/[C@H:3]1[C@H:10]([O:11][C:12](=[O:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][C@H:8]2[C@@H:4]1[CH2:5][C:6](=[O:20])[O:7]2

Participants

4

Procedure

Under an argon atmosphere, 7 g. of (1S,5R,6R,7R)-6-formyl-7-benzoyloxy-2-oxabicyclo[3,3,0]octan-3-one, E. J. Corey et al., J. Amer. Chem. Soc. 91, 5675 (1969), and 11.2 g. of [2-oxo-2-(1,3-benzodioxan-2-yl)-ethylidene]-triphenylphosphorane were agitated at room temperature for 16 hours in 300 ml. of benzene. The reaction mixture was then evaporated to dryness under vacuum. The residue was purified by column chromatography on silica gel with hexane/20-60% ethyl acetate as the eluent. Yield: 5 g. of an oil.

Workup

  1. customThe reaction mixture was then evaporated to dryness under vacuum
  2. customThe residue was purified by column chromatography on silica gel with hexane/20-60% ethyl acetate as the eluent

Sources & evidence

ORD record
ord-9f1fb030ac5c435496645533e7892150
Source dataset
uspto-grants-1980_08
Patent number
US04217360

Reaction notes

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