반응 #4549

ord-e62665853a104cb08a8caeb3781bea61

반응 방정식

CCCCCCCCc1c(Cl)nc(-c2ccc(OCCCCC[C@@H](C)CC)cc2)nc1Cl
(s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-4,6-dichloro-pyrimidine
[Mg+2].[O-2]
magnesium oxide
CCO
ethanol
CCCCCCCCc1cnc(-c2ccc(OCCCCC[C@@H](C)CC)cc2)nc1
(s)-5-n-octyl-2-[4-(6-methyloctyloxy)phenyl]-pyrimidine

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타into a 200 ml flask, then add hydrogen under oil bath conditions at 50° C., until the logical amount of hydrogen has been absorbed
  2. 2
    여과The catalyst is filtered
  3. 3
    기타separated
  4. 4
    추출ether is extracted
  5. 5
    세척After the ether layer is washed with water and with saturated salt water
  6. 6
    기타dried
  7. 7
    기타the 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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04725688uspto-grants-1988_02