반응 #60883

ord-863c4d54d6fd4c958f94e004628de8c3

반응 방정식

C[CH2][Mg][Br]
ethylmagnesium bromide
Cn1cnc(I)c1I
4,5-Diiodo-1-methyl-1H-imidazole
[Cl-].[NH4+]
NH4Cl
CCC[CH2][Sn]([Cl])([CH2]CCC)[CH2]CCC
tributyltin chloride
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1c(I)ncn1C
title compound
수율 76.0%
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1c(I)ncn1C
5-Tributylstannyl-4-iodo-1-methyl-1H-imidazole
수율 76.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe resulting clear solution was stirred for 1 hr
  2. 2
    추출The reaction mixture was extracted with DCM (500 mL)
  3. 3
    세척washed with water (3×300 mL)
  4. 4
    건조dried (MgSO4)
  5. 5
    여과filtered
  6. 6
    농축concentrated in vacuo
  7. 7
    기타The crude product was purified by flash chromatography on silica eluting with hexane:EtOAc (1:1)

실험 절차

4,5-Diiodo-1-methyl-1H-imidazole (40.0 g) was stirred in anhydrous THF (560 mL) at ambient temperature and ethylmagnesium bromide (3M in ether, 42.0 mL) was added over 20 minutes under an inert atmosphere. The resulting white precipitate was stirred for 30 minutes then tributyltin chloride (34.2 mL) added dropwise. The resulting clear solution was stirred for 1 hr, then saturated aqueous NH4Cl (50 mL) and water (300 mL) were added. The reaction mixture was extracted with DCM (500 mL), washed with water (3×300 mL), dried (MgSO4), filtered and concentrated in vacuo. The crude product was purified by flash chromatography on silica eluting with hexane:EtOAc (1:1) to afford the title compound as a colourless oil (45.1 g, 76%);

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07427616B2uspto-grants-2008_09