Hydride → HCID 19917128, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:7]=[C:8]([CH:19]=[CH:20][CH:21]=2)[O:9][CH2:10][CH2:11][O:12][CH:13]([CH3:18])[C:14](OC)=[O:15])=[CH:2]1.[Li].[H-]>O1CCCC1>[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:7]=[C:8]([CH:19]=[CH:20][CH:21]=2)[O:9][CH2:10][CH2:11][O:12][CH:13]([CH3:18])[CH2:14][OH:15])=[CH:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
0.20 g of the resulting ester compound was dissolved in 5 ml of tetrahydrofuran, and reduced as in Referential Example 31 with 25 mg of lithium alminum hydride to give 0.18 g of the captioned compound as a colorless oil.
Sources & evidence
- ORD record
- ord-ed26bd89c5cd478c909657717874124e
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05306728
Reaction notes
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