반응 #1256

ord-8266c5cd4a68414b8c3137da7bc01eef

반응 방정식

[BH4-].[Na+]
sodium borohydride
CCCCCCCCCCOc1cnc(-c2ccc(C(C)=O)cc2)nc1
2-(4-acetylphenyl)-5-decyloxypyrimidine
CCO
ethanol
ClC(Cl)Cl
chloroform
CCCCCCCCCCOc1cnc(-c2ccc(C(C)O)cc2)nc1
2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine
수율 100.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타equipped with a stirrer
  2. 2
    기타The resulting reaction mixture
  3. 3
    추출followed by extraction and liquid separation
  4. 4
    세척the obtained chloroform layer was washed with water
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    농축concentrated under reduced pressure

실험 절차

35.5 g (0.1 mo1) of 2-(4-acetylphenyl)-5-decyloxypyrimidine, 300 ml of ethanol and 300 ml of chloroform were supplied into a four-necked flask equipped with a stirrer and a thermometer. Then 2.8 g (0.075 mol) of sodium borohydride was added at 30°-40° C. and the mixture was stirred at the same temperature for 4 hours. The resulting reaction mixture was poured into 500 ml of water, followed by extraction and liquid separation, and the obtained chloroform layer was washed with water, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 35.8 g of 2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine (II-c-11) (yield: 100%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723610uspto-grants-1998_03