반응 #336544

ord-1e151b80cce54d7f8d1d8b0caaeede1c

반응 방정식

Cl.ClCn1cnc2ccccc21
1-chloromethylbenzimidazole hydrochloride
Oc1ccc(Oc2ccccc2)cc1
p-phenoxyphenol
[H-].[Na+]
sodium hydride
[H][H]
hydrogen
c1ccc(Oc2ccc(OCn3cnc4ccccc43)cc2)cc1
1-[(p-phenoxyphenoxy)-methyl]-benzimidazole
수율 49.8%

반응 조건

온도
120°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타At room temperature
  2. 2
    기타(about 20° C.)
  3. 3
    농축After concentration under reduced pressure
  4. 4
    세척washed three times with water and three times with 5% strength aqueous sodium hydroxide solution
  5. 5
    건조The combined organic phases are dried over sodium sulfate
  6. 6
    농축concentrated
  7. 7
    기타The residue is recrystallized from diethyl ether

실험 절차

At room temperature (about 20° C.) and under a nitrogen blanket, 13.95 g of p-phenoxyphenol in 100 ml of anhydrous dimethylformamide is dripped into 6.75 g of 80% strength sodium hydride in 50 ml of anhydrous dimethylformamide. Upon completion of hydrogen evolution, the mixture is stirred for 4 hours at 60° C. At 10° C., 15.22 g of 1-chloromethylbenzimidazole hydrochloride is then added. The mixture is stirred for 8 hours at 120° C. After concentration under reduced pressure, the residue is taken up in ethyl acetate, and washed three times with water and three times with 5% strength aqueous sodium hydroxide solution. The combined organic phases are dried over sodium sulfate and concentrated. The residue is recrystallized from diethyl ether. There is obtained 11.8 g of 1-[(p-phenoxyphenoxy)-methyl]-benzimidazole of m.p. 112° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05214064uspto-grants-1993_05