Réaction #1555

Équation de réaction

5,6-diethyl-2-(3-formyl-phenyl)-3-propargyl-4(3H)-pyrimidinone

hydroxylamine hydrochloride

→

5,6-diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone

Rendement 77.6%

5,6-Diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone

Rendement 77.6%

Solvants

ethanol

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture was refluxed for 17 hours
2. 2
   AutreThe ethanol was removed in vacuo and ether and ethyl acetate
3. 3
   workup.ADDITIONwere added to the residue
4. 4
   LavageThe organics were washed 3 times with water
5. 5
   Filtrationfiltered
6. 6
   Autreto remove 0.22 g of 5,6-diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone (compound 139)
7. 7
   SéchageThe organic layer was dried over MgSO4
8. 8
   Concentrationconcentrated

Mode opératoire

To a 100 mL RBF were charged 1.1 g (3.7 mmol) of 5,6-diethyl-2-(3-formyl-phenyl)-3-propargyl-4(3H)-pyrimidinone, 0.52 g (7.5 mmol) of hydroxylamine hydrochloride and 50 mL of ethanol. The reaction mixture was refluxed for 17 hours. The ethanol was removed in vacuo and ether and ethyl acetate were added to the residue. The organics were washed 3 times with water. The organic layer was gravity filtered to remove 0.22 g of 5,6-diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone (compound 139). The organic layer was dried over MgSO4 and concentrated to yield a further 0.67 g of 5,6-diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone (compound 139) as a white solid. A combined yield of 77.6% was obtained. 1H-NMR (CDCl3) 1.25(6H,m); 2.35(1H,t); 2.65(4H,m); 4.6(2H,d); 7.49-8.15(4H,m); 8.7(1H,s)

Source