Potassium Hydroxide → HCID 21452972, compound
Reaction equation
[CH:1]1([O:7][C:8]2[CH:16]=[CH:15][C:11]([C:12](Cl)=[O:13])=[CH:10][CH:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]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>[CH:1]1([O:7][C:8]2[CH:16]=[CH:15][C:11]([C:12]([NH:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][NH:25][C:12](=[O:13])[C:11]3[CH:15]=[CH:16][C:8]([O:26][CH:1]4[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]4)=[CH:9][CH:10]=3)=[O:13])=[CH:10][CH:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
m.p. 144°-145° C., 27.3 g., was prepared as in Example 1 using 4-cyclohexyloxybenzoyl chloride (from 42.0 g. of the corresponding acid as in Example 6) in 100 ml. of ethylene dichloride, 11.7 g. of 1,7-heptanediamine, 200 ml. of 10% 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-8ecfb056574b46a1968ff77015dfd94c
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04009208
Reaction notes
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