Ethyl Acetate → HCID 293025, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]=1[C:13](C)=[CH:14][C:15](O)=O.[C:19]([O:22]CC)(=[O:21])C>[Pd]>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]=1[CH2:13][CH2:14][CH2:15][C:19]([OH:22])=[O:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound obtained in Step A (3.4 g, 1.40.10−2 mol) is solubilised in ethyl acetate (90 ml) in the presence of 5% palladium-on-carbon. The mixture is purged with argon and placed under a hydrogen atmosphere. After 15 hours' hydrogenation, the reaction mixture is filtered over Celite, rinsed and then evaporated under reduced pressure. The title product is isolated in the form of white crystals.
Workup
- customThe mixture is purged with argon
- filtrationthe reaction mixture is filtered over Celite
- washrinsed
- customevaporated under reduced pressure
Sources & evidence
- ORD record
- ord-e6b0585a1cd648f7b0d6331860d9d1d2
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06423870B1
Reaction notes
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