Aluminum(III) Chloride → 6-(3-Carbomethoxy-2-methyl-propionyl)-3,4-dihydro-2(1H)-quinazolinone

HRID 1607986

Reaktionsgleichung

Reaktionsgleichung von HRID 1607986
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][NH:3][C:2]1=[O:11].[Cl-].[Al+3].[Cl-].[Cl-].[C:16]([CH2:20][CH:21]([CH3:25])[C:22](Cl)=[O:23])([O:18][CH3:19])=[O:17]>C(=S)=S>[C:16]([CH2:20][CH:21]([CH3:25])[C:22]([C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[NH:1][C:2](=[O:11])[NH:3][CH2:4]2)=[O:23])([O:18][CH3:19])=[O:17]

Komponenten

5

Versuchsvorschrift

3,4-Dihydro-2(1H)-quinazolinone (3.6 g) is added to a stirred suspension of anhydrous aluminum chloride (16.5 g) in carbon disulfide (120 ml) under nitrogen. 3-Carbomethoxy-2-methyl-propionyl chloride (4 g) is added dropwise tothe stirred suspension, and the reaction mixture refluxed for about 18 hours, cooled to RT and further cooled to 0° C. in an ice bath. The liquid phase is decanted and ice and cold water slowly added to the residue. The aqueous mixture is filtered and the filtered solid suspended and stirred in the anhydrous diethyl ether overnight. The suspension is filtered and the filtered solid used in the next step without further purification.

Aufarbeitung

  1. temperaturethe reaction mixture refluxed for about 18 hours
  2. temperaturefurther cooled to 0° C. in an ice bath
  3. customThe liquid phase is decanted
  4. additionice and cold water slowly added to the residue
  5. filtrationThe aqueous mixture is filtered
  6. stirringstirred in the anhydrous diethyl ether overnight
  7. filtrationThe suspension is filtered
  8. customthe filtered solid used in the next step without further purification

Quellen und Nachweise

ORD-Eintrag
ord-8475f41054b242c1abea36b8d95d2000
Quelldatensatz
uspto-grants-1989_09
Patentnummer
US04868300

Verknüpfte Notizen

Wird geladen…