Ethyl Acetate → HCID 21620084, compound
Reaction equation
[N:1]1([CH2:6][C:7](C2C=CC(C#N)=CC=2)=[CH:8][C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=2)[CH:5]=[N:4][CH:3]=[N:2]1.[H][H].C(O[CH2:33][CH3:34])(=O)C>[Pd]>[N:1]1([CH2:6][CH:7]([C:34]2[CH:33]=[CH:10][CH:9]=[CH:8][C:7]=2[C:6]#[N:1])[CH2:8][C:9]2[CH:10]=[CH:11][C:12]([C:15]([F:16])([F:17])[F:18])=[CH:13][CH:14]=2)[CH:5]=[N:4][CH:3]=[N:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-[1-(1,2,4-triazol-1-ylmethyl)-2-(4-trifluoromethylphenyl)vinyl]benzonitrile (0.05 g, mixed E and Z isomers) and 10% by weight palladium-on-carbon (0.02 g) in ethyl acetate (5 ml) was stirred rapidly under an atomosphere of hydrogen at atmospheric pressure for 2h. The mixture was filtered, and the filtrate was evaporated to dryness, to give 4-([2-(1,2,4-triazol-1-yl)-1-(4-trifluoromethylbenzyl)ethyl]benzonitrile as a white solid, which was washed with ethyl acetate and dried, m.p. 123°.
Workup
- filtrationThe mixture was filtered
- customthe filtrate was evaporated to dryness
Sources & evidence
- ORD record
- ord-13bd1ddd07dc4b059f8e0019297bb097
- Source dataset
- uspto-grants-1991_04
- Patent number
- US05006543
Reaction notes
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