Sodium Methoxide → 2-(Trifluoromethyl)pyrimidin-5-ol

Temperature

121 °C

2-(Trifluoromethyl)-1,4,5,6-tetrahydropyrimidin-5-ol (4.20 g, 25 mmol) was stirred in nitrobenzene at 90° C. Sodium methoxide (5.4 g, 100 mmol) was dissolved in methanol (75 ml) and added portionwise to the reaction mixture, allowing the methanol to distill off before the next addition. The reaction mixture was then warmed to 121° C. for one hour, cooled, shaken with water (150 ml), the organic phase separated off and the aqueous phase washed with ethyl acetate (2×100 ml). The aqueous phase was adjusted to pH 4.0 with 6M aqueous hydrochloric acid, extracted with ethyl acetate (2×100 ml), dried and evaporated to give 2.53 g (61.7%) of an orange coloured product that was used without further purification.

1. additionadded portionwise to the reaction mixture
2. distillationto distill off before the next addition
3. temperaturecooled
4. customthe organic phase separated off
5. washthe aqueous phase washed with ethyl acetate (2×100 ml)
6. extractionextracted with ethyl acetate (2×100 ml)
7. customdried
8. customevaporated

ORD record

ord-ab7a8f3db8f742339c08371e3b1246ed

Source dataset

uspto-grants-2012_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08183251B2