Water → 50889-48-0

HRID 1159579Notes

Reaction equation

HRID 1159579 reaction equation
[F:1][C:2]([F:16])([CH2:12][CH2:13][CH2:14][CH3:15])[C:3](=[O:11])[CH2:4]P(=O)(OC)OC.[H-].[Li+].[O:19]=[C:20]1[O:24][C@H:23]2[CH2:25][C@@H:26]([O:30][C:31]([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)=[O:32])[C@H:27]([CH:28]=O)[C@H:22]2[CH2:21]1.O>COC(C)(C)C>[F:16][C:2]([F:1])([CH2:12][CH2:13][CH2:14][CH3:15])[C:3](=[O:11])/[CH:4]=[CH:28]/[C@@H:27]1[C@@H:22]2[C@@H:23]([O:24][C:20](=[O:19])[CH2:21]2)[CH2:25][C@H:26]1[O:30][C:31]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:32]

Participants

6

Reactant 4

HCID 962WaterHCID 62714Lithium hydrideHCID 11000244(3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoateHCID 11118722Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate

Product 1

HCID 6848260050889-48-0Yield 4.8%

Reagents, catalysts & solvents 1

HCID 15413tert-Butyl methyl etherSolvent

Procedure

To a solution of dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate (1) (0.969 g, 3.75 mmol) in anhydrous t-butyl methyl ether (15 ml), lithium hydride (28.6 mg, 3.60 mmol) was added and the mixture was stirred for two hours at room temperature. (3aR,4R,5R,6aS)-2-oxo-5-phenylcarbonyloxyhexahydrocyclopenta[b]furan-4-carbaldehyde (10) (0.686 g, 2.50 mmol) was added thereto and the mixed solution was stirred for approximately 6 hours at room temperature. Water was added to the solution and the mixture was stirred, let to stand and then separated into two layers. The aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, sequentially washed with 3% aqueous sodium chloride and saturated aqueous sodium chloride, and then dried with anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (Fuji Silysia RW-300SP: 28 g; ethyl acetate:hexane=1:2) to give (3aR,4R,5R,6aS)-4-((E)-4,4-difluoro-3-oxo-1-octenyl)-2-oxo-5-phenylcarbonyloxyhexahydrocyclopenta[b]furan (11) (48.5 mg; 0.119 mmol; yield: 4.8%).

Workup

  1. stirringthe mixed solution was stirred for approximately 6 hours at room temperature
  2. stirringthe mixture was stirred
  3. customseparated into two layers
  4. extractionThe aqueous layer was extracted twice with ethyl acetate
  5. washsequentially washed with 3% aqueous sodium chloride and saturated aqueous sodium chloride
  6. dry with materialdried with anhydrous magnesium sulfate
  7. concentrationAfter concentration under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (Fuji Silysia RW-300SP: 28 g; ethyl acetate:hexane=1:2)

Sources & evidence

ORD record
ord-143a8c2d258c45949dc02db28d91c70c
Source dataset
uspto-grants-2010_10
Patent number
US07812182B2

Reaction notes

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