Sodium Carbonate → (3aRS,5RS,7aRS)-5-acetoxy-2-benzyl-7,7-diphenylperhydro-4-isoindolone
Reaction equation
[C:1]([O:4][CH:5]1[C:10](=[O:11])[CH:9]=[CH:8][C:7]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:6]1)(=[O:3])[CH3:2].C(O[CH2:29][N:30]([CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)[CH2:31][Si](C)(C)C)CCC.C(=O)([O-])[O-].[Na+].[Na+]>ClCCl.FC(F)(F)C(O)=O>[C:1]([O:4][CH:5]1[CH2:6][C:7]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:8]2[CH:9]([CH2:29][N:30]([CH2:36][C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)[CH2:31]2)[C:10]1=[O:11])(=[O:3])[CH3:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 86 g of 6-acetoxy-4,4-diphenyl-2-cyclohexenone and 96 cm3 of N-butoxymethyl-N-(trimethylsilylmethyl)benzylamine in 1000 cm3 of dichloromethane are added 15 drops of trifluoroacetic acid. The reaction mixture is stirred at room temperature for 15 hours, followed by addition of 2 g of sodium carbonate and concentration to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of Merck silica gel (particle size 0.04-0.06 mm, diameter 7 cm, height 70 cm), eluting under a nitrogen pressure of 50 kPa with a mixture of cyclohexane and ethyl acetate (20/80 by volume) and collecting 200 cm2 fractions. Fractions 6 to 10 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 70 g of (3aRS,5RS,7aRS)-5-acetoxy-2-benzyl-7,7-diphenylperhydro-4-isoindolone in the form of a syrup are obtained (melting point below 40° C.).
Workup
- customThe residue is chromatographed on a column of Merck silica gel (particle size 0.04-0.06 mm, diameter 7 cm, height 70 cm)
- washeluting under a nitrogen pressure of 50 kPa
- additionwith a mixture of cyclohexane and ethyl acetate (20/80 by volume)
- customcollecting 200 cm2 fractions
- concentrationconcentrated to dryness under reduced pressure (2.7 kPa)
Sources & evidence
- ORD record
- ord-913a6feed96a437ebd28023f775cac77
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05631279
Reaction notes
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