Ammonium Hydroxide → HCID 136045442, compound
Reaction equation
[F:1][C:2]1[CH:23]=[CH:22][CH:21]=[CH:20][C:3]=1[C:4]([C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[C:13]1[C:14]([C:18]#[N:19])=[CH:15][NH:16][CH:17]=1)=O.[OH-].[NH4+]>[Ni].C(O)(=O)C>[Cl:12][C:10]1[CH:9]=[CH:8][C:7]2[C:13]3[C:14](=[CH:15][NH:16][CH:17]=3)[CH2:18][N:19]=[C:4]([C:3]3[CH:20]=[CH:21][CH:22]=[CH:23][C:2]=3[F:1])[C:6]=2[CH:11]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 3.0 g (9 mmole) of 4-[2-(2-fluorobenzoyl)-4-chlorophenyl]-1H-pyrrole-3-carbonitrile, ca 3 g of Raney nickel and 150 ml of glacial acetic acid was hydrogenated on a Parr apparatus at 50 psi for 6 hr. The Raney nickel was removed by filtration, and the acetic acid was removed at reduced pressure to give a yellow oil. The yellow oil was poured over ice, basified with ammonium hydroxide and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to give tan crystals. Recrystallization from a mixture of ether and methylene chloride gave cream prisms, mp 197°-199°.
Workup
- customThe Raney nickel was removed by filtration
- customthe acetic acid was removed at reduced pressure
- customto give a yellow oil
- additionThe yellow oil was poured over ice
- extractionextracted with methylene chloride
- dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure
- customto give tan crystals
- customRecrystallization
- additionfrom a mixture of ether and methylene chloride
- customgave cream prisms, mp 197°-199°
Sources & evidence
- ORD record
- ord-7a287aed1dcd4e758fe7896ccebb9b65
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04354973
Reaction notes
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