HCID 131719272, compound → HCID 131719274, compound
Reaction equation
[Si:1]([O:8][C:9]1[C:17]([CH2:18]/[CH:19]=[C:20](\[CH3:39])/[CH:21]([CH2:28][CH2:29][CH2:30][O:31][Si](C(C)(C)C)(C)C)[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:16]([O:40][CH3:41])[C:15]([CH3:42])=[C:14]2[C:10]=1[C:11](=[O:43])[O:12][CH2:13]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]>C(#N)C>[Si:1]([O:8][C:9]1[C:17]([CH2:18]/[CH:19]=[C:20](\[CH3:39])/[CH:21]([CH2:28][CH2:29][CH2:30][OH:31])[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:16]([O:40][CH3:41])[C:15]([CH3:42])=[C:14]2[C:10]=1[C:11](=[O:43])[O:12][CH2:13]2)([C:4]([CH3:5])([CH3:7])[CH3:6])([CH3:3])[CH3:2]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl (E) 6-(4-tert-butyldimethylsilyloxy-1,3-dihydro-6-methoxy-7-methyl-3-oxo-isobenzofuran-5-yl)-3-(3-tert-butyldimethylsilyloxypropyl)-4-methylhex-4-enoate (2.92 g) was dissolved in acetonitrile (50 ml). To this was added a solution of 40% aqueous HF (5 ml) in acetonitrile (45 ml), and the reaction mixture stirred for 10 minutes. Most of the acetonitrile was then evaporated, and the remaining solution diluted with ether. The ether was washed with water, saturated sodium bicarbonate (3X), brine, and dried. Evaporation of the solvent gave an oil which was chromatographed on silica gel (40% ethyl acetate in hexmnes) to give ethyl (E) 6-(4-tert-butyldimethylsilyloxy-1,3-dihydro-6-methoxy-7-methyl-3-oxo-isobenzofuran-5-yl)-3-(3-hydroxypropyl)-4-methylhex-4-enoate (2.10 g), a compound of Formula 803, as an oil.
Workup
- customMost of the acetonitrile was then evaporated
- additionthe remaining solution diluted with ether
- washThe ether was washed with water, saturated sodium bicarbonate (3X), brine
- customdried
- customEvaporation of the solvent
- customgave an oil which
- customwas chromatographed on silica gel (40% ethyl acetate in hexmnes)
Sources & evidence
- ORD record
- ord-3b3eda44da56444ba0ed8cba3e3f8bfb
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05493030
Reaction notes
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