تفاعل #2487290

معادلة التفاعل

phosphorous pentoxide

2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone

dimethoxymethane

phosphorous pentoxide

sodium hydroxide

→

3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone

المردود 32.8%

المذيبات

chloroform

methylene chloride

hexane

ethyl acetate

ظروف التفاعل

المعالجة

1. 1
   أخرىat room temperature
2. 2
   workup.ADDITIONThe reaction mixture was poured
3. 3
   workup.ADDITIONwere added
4. 4
   أخرىThe layers were separated
5. 5
   استخلاصthe aqueous layer was extracted twice with methylene chloride
6. 6
   غسيلwashed with brine
7. 7
   تجفيفdried over MgSO4
8. 8
   تركيزconcentrated
9. 9
   أخرىto yield 1.1 g crude product, which
10. 10
    أخرىwas purified by recrystallization from hexane

الإجراء التجريبي

To a solution of 1.5 g (5.9 mmol) of 2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone, 17.2 g (226.3 mmol) dimethoxymethane, and 35 mL of chloroform was added 2.5 g (17.6 mmol) phosphorous pentoxide, at room temperature. By TLC (25% ethyl acetate in hexane) the reaction was incomplete after 4 h and an additional 3 g (21.1 mmol) phosphorous pentoxide was added. Stirring was continued for 16 h. The reaction mixture was poured onto crushed ice and 1M sodium hydroxide and methylene chloride were added. The layers were separated and the aqueous layer was extracted twice with methylene chloride. The organic extracts were combined and washed with brine, then dried over MgSO4 and concentrated to yield 1.1 g crude product, which was purified by recrystallization from hexane. Thus, 0.55 g (32%) 3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone (Compound 6) as a yellow solid was obtained. 1H-NMR (CDCl3)δ3.55 (3 H, s); 5.2 (2H, d); 6.85 (1H, s); 7.65 (3H, m); 7.75 (2H, m).

المصدر