Sodium borohydride → HCID 10821610, compound
Reaction equation
[BH4-].[Na+].[C:3]1(=[CH:15][C:16]#[N:17])[C:13]2=[C:14]3[C:9](=[CH:10][CH:11]=[CH:12]2)[CH:8]=[CH:7][CH:6]=[C:5]3[CH2:4]1>CO.Cl[Pd]Cl>[CH:3]1([CH2:15][C:16]#[N:17])[C:13]2=[C:14]3[C:9](=[CH:10][CH:11]=[CH:12]2)[CH:8]=[CH:7][CH:6]=[C:5]3[CH2:4]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The catalyst is prepared starting from 55 mg of PdCl2 in 5 ml of methanol treated with 25 mg of sodium borohydride. After 15 minutes' stirring, the compound obtained in Step A (1 g, 5.23.10−3 mol), diluted with methanol (15 ml), is incorporated. The mixture is purged with argon and placed under hydrogen. After 3 days' hydrogenation, the reaction mixture is filtered over Celite, rinsed and then evaporated under reduced pressure. The title product is isolated in the form of a light brown oil.
Workup
- customThe catalyst is prepared
- customThe mixture is purged with argon
- waitAfter 3 days' hydrogenation
- filtrationthe reaction mixture is filtered over Celite
- washrinsed
- customevaporated under reduced pressure
Sources & evidence
- ORD record
- ord-093f7d6e7ef945e89e87a5ba4ae8000a
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06423870B1
Reaction notes
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