Allyl bromide → HCID 15018887, Verbindung
Reaktionsgleichung
C(=O)([O-])[O-].[K+].[K+].[CH2:7](Br)[CH:8]=[CH2:9].[OH:11][C:12]1[CH:13]=[C:14]([N:18]2[C:22](=[O:23])[C:21]3[CH2:24][CH2:25][CH2:26][CH2:27][C:20]=3[C:19]2=[O:28])[CH:15]=[CH:16][CH:17]=1>CC(C)=O>[CH2:7]([O:11][C:12]1[CH:13]=[C:14]([N:18]2[C:19](=[O:28])[C:20]3[CH2:27][CH2:26][CH2:25][CH2:24][C:21]=3[C:22]2=[O:23])[CH:15]=[CH:16][CH:17]=1)[CH:8]=[CH2:9]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3.0 g of powdered potassium carbonate, then 2.6 g of allyl bromide were added to a stirred suspension of 5.0 g of 1A in 25 mL of acetone. The mixture was refluxed for 1 hour, then stirred overnight at room temperature. The solvent was evaporated, water was added to the residue and the pH of the mixture was adjusted to 11 by addition of 10% aqueous sodium hydroxide. The resulting mixture was extracted with ethyl acetate, the extract was washed with brine and dried (Na2SO4), the solvent was evaporated and the residue was flash chromatographed on silica gel with a 1:9 v:v mixture of ethyl acetate and hexane as eluent to give N-(3-allyloxyphenyl)-3,4,5,6-tetrahydrophthalimide (1B), as yellow crystals, m.p.: 88°-90° C.
Aufarbeitung
- temperatureThe mixture was refluxed for 1 hour
- customThe solvent was evaporated
- additionwater was added to the residue
- additionthe pH of the mixture was adjusted to 11 by addition of 10% aqueous sodium hydroxide
- extractionThe resulting mixture was extracted with ethyl acetate
- washthe extract was washed with brine
- dry with materialdried (Na2SO4)
- customthe solvent was evaporated
- customchromatographed on silica gel with a 1:9 v
- additionv mixture of ethyl acetate and hexane as eluent
Quellen und Nachweise
- ORD-Eintrag
- ord-2ce149da1a7c47b2bbf860758b4551b3
- Quelldatensatz
- uspto-grants-1989_11
- Patentnummer
- US04881967
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