Reaktionsgleichung
[OH:1][CH2:2][CH2:3][N:4]=[C:5]([OH:33])[C:6]1[C:7](=[C:11](Cl)[C:12]([S:24][C:25]2[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=2)=[C:13]([S:16][C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)[C:14]=1Cl)[C:8]([OH:10])=[O:9].[CH2:34]([SH:44])[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[OH:1][CH2:2][CH2:3][N:4]=[C:5]([OH:33])[C:6]1[C:7](=[C:11]([S:44][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[C:12]([S:24][C:25]2[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=2)=[C:13]([S:16][C:17]2[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=2)[C:14]=1[S:44][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[C:8]([OH:10])=[O:9]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2 g (3.95 millimols) of 4,5-bis-(p-tolylthio)-3,6-dichlorophthalic acid N-2-hydroxyethylimide, 1,51 g (8.69 millimols) of n-decane-1-thiol, 2.29 g (16.58 millimols) of potassium carbonate and 20 ml of N,N-dimethylformamide are stirred at 25° C. for 1 hour. After concentration, the residue is taken up in methylene chloride/dilute HCl solution. The extracts are dried over sodium sulfate and evaporated. After precipitation from n-hexane, 300 mg (10% of theory) of the title compound (waxy substance) are obtained.
Aufarbeitung
- concentrationAfter concentration
- dry with materialThe extracts are dried over sodium sulfate
- customevaporated
- customAfter precipitation from n-hexane, 300 mg (10% of theory) of the title compound (waxy substance)
- customare obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-1302995189ae4247b2f82eaa3f97a735
- Quelldatensatz
- uspto-grants-1985_08
- Patentnummer
- US04537977
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