반응 #1447106

ord-2349a904db3a4ca4b48f369c94d878ac

반응 방정식

FB(F)F
boron trifluoride
[K+].[OH-]
KOH
CC(C)OC(C)C
diisopropylether
CCc1ccc(C(=O)c2cc(I)cc(Br)c2C)cc1
(3-bromo-5-iodo-2-methyl-phenyl)-(4-ethyl-phenyl)-methanone
CC[SiH](CC)CC
triethylsilane
CCc1ccc(Cc2cc(I)cc(Br)c2C)cc1
3-Bromo-5-(4-ethyl-benzyl)-1-iodo-4-methyl-benzene

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONare added
  2. 2
    기타The organic phase is separated
  3. 3
    추출the aqueous phase is extracted three times with diisopropylether
  4. 4
    세척The combined organic phases are washed with 2 M potassium hydroxide solution and brine
  5. 5
    건조dried (sodium sulphate)
  6. 6
    기타After the solvent is evaporated
  7. 7
    기타the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 1:0->1:1)

실험 절차

A solution of (3-bromo-5-iodo-2-methyl-phenyl)-(4-ethyl-phenyl)-methanone (4.2 g) and triethylsilane (4.7 mL) in dichloromethane (10 mL) and acetonitrile (28 mL) is cooled in an ice-bath. Then, boron trifluoride diethyletherate (1.4 mL) is added dropwise over 3 min. The solution is stirred for 14 h at ambient temperature, before an aqueous 25% solution of KOH and diisopropylether are added. The organic phase is separated and the aqueous phase is extracted three times with diisopropylether. The combined organic phases are washed with 2 M potassium hydroxide solution and brine and then dried (sodium sulphate). After the solvent is evaporated, the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 1:0->1:1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07879807B2uspto-grants-2011_02