반응 #1166464

ord-7562b3561b1a410caa8564ca15ef695d

반응 방정식

CCCCOc1c(OC(C)=O)c(=O)oc2cc(OC(C)=O)ccc12
4-butoxy-3, 7-diacetoxy-2H-l-benzopyran-2-one
C[O-].[Na+]
sodium methoxide
CCCCOc1c(OC(C)=O)c(=O)oc2cc(O)ccc12
title compound
수율 85.0%
CCCCOc1c(OC(C)=O)c(=O)oc2cc(O)ccc12
3-acetoxy-4-butoxy-7-hydroxy-2H-1-benzopyran-2-one
수율 85.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThen 22.36 g of Amberlyst-15 was added
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hour
  3. 3
    여과Amberlyst-15 was filtered off
  4. 4
    농축the filtrate was concentrated under reduced pressure
  5. 5
    기타to give a crystalline product
  6. 6
    기타The product was reprecipitated from tertahydrofuran and hexane

실험 절차

To a mixture of 17.31 g of 4-butoxy-3, 7-diacetoxy-2H-l-benzopyran-2-one (51.79 mmol) in 170 ml of methanol was added 2.66 g of sodium methoxide (49.20 mmol) and the reaction mixture was stirred at room temperature for 3 hours. Then 22.36 g of Amberlyst-15 was added, and the mixture was stirred at room temperature for 1 hour. Amberlyst-15 was filtered off and the filtrate was concentrated under reduced pressure to give a crystalline product. The product was reprecipitated from tertahydrofuran and hexane to give 12.87 g of the title compound. (yield=85%)

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05580552uspto-grants-1996_12