Potassium Hydroxide → HCID 21453014, compound
Reaction equation
[Cl:1][CH:2]([F:16])[C:3]([F:15])([F:14])[O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=[O:10])=[CH:7][CH:6]=1.[CH2:17]([NH2:25])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][NH2:24].[OH-:26].[K+]>C(Cl)CCl>[Cl:1][CH:2]([F:16])[C:3]([F:15])([F:14])[O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([NH:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][NH:25][C:9](=[O:10])[C:8]2[CH:7]=[CH:6][C:5]([O:26][C:3]([F:14])([F:15])[CH:2]([F:16])[Cl:1])=[CH:13][CH:12]=2)=[O:10])=[CH:7][CH:6]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
m.p. 153°-154° C., 16.0 g., was prepared as in Example 16 using 4-(2-chloro-1,1,2-trifluoroethoxy)benzoyl chloride (from 23.0 g. of the corresponding acid as in Example 16) in 150 ml. of ethylene dichloride, 5.8 g. of 1,7-heptanediamine, 200 ml. of 10% aqueous potassium hydroxide solution, 500 ml. of ethylene dichloride and recrystallization from acetonitrile using decolorizing charcoal.
Workup
- customof ethylene dichloride and recrystallization from acetonitrile using
Sources & evidence
- ORD record
- ord-10c26637b96e40219c9efffbde17d349
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04009208
Reaction notes
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