Sodium Acetate → HCID 18177413, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[O:9][CH2:8][CH2:7][CH:6]2[C:13]#[N:14].[C:15]([O-])(=[O:17])[CH3:16].[Na+]>C(OC(=O)C)(=O)C.[Ni]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[O:9][CH2:8][CH2:7][CH:6]2[CH2:13][NH:14][C:15](=[O:17])[CH3:16]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The nitrile obtained in Step A (200 mg; 1.05 mmol) is solubilised in the reactor of a Parr apparatus in 15 ml of acetic anhydride. Raney nickel (60 mg; 30% by weight) and also sodium acetate (1.5 eq; 1.58 mmol; 130 mg) are added. The reactor is placed under hydrogen pressure of 580 psi at 50° C. for 12 hours. When the reaction is complete, filtration over Celite and then rinsing with AcOEt are carried out. The product is purified by flash chromatography on silica gel (eluant:AcOEt (100%)). The white solid obtained is recrystallised from a pentane-ether mixture.
Workup
- customat 50° C.
- customfor 12 hours
- filtrationfiltration over Celite
- washrinsing with AcOEt
- customThe product is purified by flash chromatography on silica gel (eluant:AcOEt (100%))
- customThe white solid obtained
- customis recrystallised from a pentane-ether mixture
Sources & evidence
- ORD record
- ord-d36826f60bdd493195b52e00e7b8b413
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313160B1
Reaction notes
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