반응 #4549
ord-e62665853a104cb08a8caeb3781bea61
반응 방정식
(s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-4,6-dichloro-pyrimidine
magnesium oxide
ethanol
→
(s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-pyrimidine
용매
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타into a 200 ml flask, then add hydrogen under oil bath conditions at 50° C., until the logical amount of hydrogen has been absorbed
- 2여과The catalyst is filtered
- 3기타separated
- 4추출ether is extracted
- 5세척After the ether layer is washed with water and with saturated salt water
- 6기타dried
- 7기타the ether is evaporated
실험 절차
Pour 1.88 g of optically active (s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-4,6-dichloro-pyrimidine, 0.4 g of 10% palladium-carbon, 0.55 g of magnesium oxide, 60 ml of ethanol, and 45 ml of water, into a 200 ml flask, then add hydrogen under oil bath conditions at 50° C., until the logical amount of hydrogen has been absorbed. The catalyst is filtered and separated, then ether is extracted. After the ether layer is washed with water and with saturated salt water, and dried, the ether is evaporated. The resultant impure product is repeatedly refined, and 0.9 g of optically active (s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-pyrimidine is obtained.