반응 #2025294

ord-297227e609b347969998ac9d55ff14cf

반응 방정식

[Na+].[OH-]
sodium hydroxide
CO
methanol
CCCCCCCCCCOc1cnc(-c2ccc(C(C)OC(C)=O)cc2)nc1
(-)-2-{4-(1-acetoxyethyl)phenyl}-5-decyloxypyrimidine
Cl
hydrochloric acid
CCCCCCCCCCOc1cnc(-c2ccc(C(C)O)cc2)nc1
(-)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine
수율 98.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to subject to reaction at 40° to 45° C. for 4 hours
  2. 2
    workup.ADDITIONwas added to the reaction mixture
  3. 3
    세척After the organic phase was washed with water
  4. 4
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure

실험 절차

Into 100 ml of methanol and 50 ml of tetrahydrofuran were dissolved 15 g of the (-)-2-{4-(1-acetoxyethyl)phenyl}-5-decyloxypyrimidine obtained in Preparation Example [starting material compound (VI)] 70, and then 50 ml of 20% aqueous sodium hydroxide solution were added thereto, to subject to reaction at 40° to 45° C. for 4 hours. After completion of the reaction, 4N hydrochloric acid was added to the reaction mixture to adjust it to pH 7 to 8, and then 200 ml of toluene were added to effect extraction and separation. After the organic phase was washed with water, the solvent was distilled off under reduced pressure to obtain 13.2 g (yield: 98.5%) of (-)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05693251uspto-grants-1997_12