Sodium hydride → HCID 22235060, compound
Reaction equation
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:14]=[CH:13][C:6]([CH2:7][CH:8]([C:11]#[N:12])[C:9]#[N:10])=[CH:5][CH:4]=1.[H-].[Na+].Br[CH2:20][CH2:21][CH2:22][CH2:23][Cl:24]>CN(C)C=O>[Cl:24][CH2:23][CH2:22][CH2:21][CH2:20][C:8]([CH2:7][C:6]1[CH:5]=[CH:4][C:3]([C:2]([F:15])([F:16])[F:1])=[CH:14][CH:13]=1)([C:11]#[N:12])[C:9]#[N:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Using 0.22 g of (4-(trifluoromethyl)benzyl)malononitrile, 3 ml of N,N-dimethylformamide, 0.05 g of sodium hydride (60% in oil), and 0.34 g of 1-bromo-4-chlorobutane, and according to the process described in the Production Example 1, there was obtained 0.20 g of 2-(4-chlorobutyl)-2-(4-(trifluoromethyl)benzyl)malononitrile (the present compound (87)).
Sources & evidence
- ORD record
- ord-335fc2fa0bf94a4b8a097928f312ce09
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07402691B2
Reaction notes
Loading…