Water → HCID 53915902, compound
Reaction equation
[CH3:1][C:2](=[CH:8][C:9]1[CH:13]([CH:14]([CH3:16])[CH3:15])[CH2:12][CH2:11][C:10]=1[CH3:17])[C:3](OCC)=[O:4].[H-].[H-].[H-].[H-].[Li+].[Al+3].O>CCOCC>[CH3:1][C:2](=[CH:8][C:9]1[CH:13]([CH:14]([CH3:15])[CH3:16])[CH2:12][CH2:11][C:10]=1[CH3:17])[CH2:3][OH:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
40 g of ethyl 2-methyl-3-(2-methyl-5-isopropyl-cyclopent-1-en-1-yl)-prop-2-enoate in 100 ml cooled ether were added under stirring to a suspension of 4 g of LiAlH4 in 50 ml ether. After addition of water to the thus obtained suspension, the separated organic phase was dried and evaporated to dryness. There was thus obtained 31.4 g (yield 95%) of the desired alcohol; bp. 75°-80°/0.01 Torr.
Workup
- additionwere added
- customthe separated organic phase was dried
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-f67f7b10dfe14028b33fc62c7af25173
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03978009
Reaction notes
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