Potassium Iodide → N-[4-bromo-3-(1-ethoxycarbonylbutyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12](=[O:13])[C:11]3[CH2:14][CH2:15][CH2:16][CH2:17][C:10]=3[C:9]2=[O:18])=[CH:4][C:3]=1[OH:19].Br[CH:21]([CH2:27][CH2:28][CH3:29])[C:22]([O:24][CH2:25][CH3:26])=[O:23].C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:9](=[O:18])[C:10]3[CH2:17][CH2:16][CH2:15][CH2:14][C:11]=3[C:12]2=[O:13])=[CH:4][C:3]=1[O:19][CH:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:27][CH2:28][CH3:29]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 15.0 g. of N-(4-bromo-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide, 12.0 g. of ethyl α-bromovalerate, 7.7 g. of potassium carbonate, 2.5 g. of potassium iodide and 50 ml. of acetone was refluxed with stirring for 3 hours and then, the reaction mixture was cooled to room temperature and the salt was separated by a filtration. The filtrate was concentrated under a reduced pressure and 2N-HCl was added to the residue to crystallize the product. The crystal was separated by a filtration and washed with water and dried. The residue was purified by a chromatography on a column of silica gel (developing solvent: ethyl acetate: n-hexane of 1:3) to obtain 17.6 g. of Compound No. 90 shown in table 1.
Aufarbeitung
- additionA mixture of 15.0 g
- customthe salt was separated by a filtration
- concentrationThe filtrate was concentrated under a reduced pressure and 2N-HCl
- additionwas added to the residue
- customto crystallize the product
- customThe crystal was separated by a filtration
- washwashed with water
- customdried
- customThe residue was purified by a chromatography on a column of silica gel (developing solvent: ethyl acetate: n-hexane of 1:3)
- customto obtain 17.6 g
Quellen und Nachweise
- ORD-Eintrag
- ord-4de79521328748efa30b11fa01c2c1d5
- Quelldatensatz
- uspto-grants-1985_08
- Patentnummer
- US04536209
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