Sodium hydride → 2,4,5,6,7-Pentachloro-1-(2-acetoxyethoxymethyl)benzimidazole

HRID 263893노트

반응식

HRID 263893 반응식
[H-].[Na+].[Cl:3][C:4]1[NH:5][C:6]2[C:12]([Cl:13])=[C:11]([Cl:14])[C:10]([Cl:15])=[C:9]([Cl:16])[C:7]=2[N:8]=1.[C:17]([O:20][CH2:21][CH2:22][O:23][CH2:24]Br)(=[O:19])[CH3:18]>CC#N>[Cl:3][C:4]1[N:5]([CH2:24][O:23][CH2:22][CH2:21][O:20][C:17](=[O:19])[CH3:18])[C:6]2[C:12]([Cl:13])=[C:11]([Cl:14])[C:10]([Cl:15])=[C:9]([Cl:16])[C:7]=2[N:8]=1

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 3676562-(Bromomethoxy)ethyl acetateHCID 232739742,4,5,6,7-pentachloro-1H-benzimidazole

생성물 1

HCID 186975732,4,5,6,7-Pentachloro-1-(2-acetoxyethoxymethyl)benzimidazole

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

NaH (0.12 g, 3.0 mmole, 60% oil disperson) was added to a stirred suspension of 2,4,5,6,7-pentachlorobenzimidazole (14) (1.0 g, 3.4 mmole) in dry CH3CN (120 mL) under a N2 atmosphere. The solution was stirred until H2 evolution has ceased and a clear solution was obtained (20 min.). (2-Acetoxyethoxy) methyl bromide (0.68 g, 10.66 mmole) in CH3CN (34 mL) was then added dropwise. The reaction mixture was stirred for an additional 3 hr. The resulting mixture was concentrated under reduced pressure, diluted with H2O (50 mL), extracted with EtOAc (100 mL), washed with H2O (100 mL), dried (anhyd. Na2SO4) and the solvent was removed under reduced pressure to yield an oil (165). The resulting oil was purified by flash column chromatography (2×24 cm) (230-400 mesh). Elution of the column with hexane:EtOAc (6:4, v/v) and evaporation of the appropriate fractions gave a solid which was recrystallized from MeOH to afford 1.39 g (72%) of 165: m.p. 119° C. 1H NMR (CDCl3): d 5.93 (s, 2H, C-1'), 4.143.92 (m, 4H, C-3' and C-4'), 1.83 (s, 3H, Ac). Anal. Calcd. for C12H9N2Cl5O3 : C,35.45; H, 2.23; N, 6.89. Found: C, 35.57; H, 2.17; N, 16.91.

후처리

  1. customa clear solution was obtained (20 min.)
  2. stirringThe reaction mixture was stirred for an additional 3 hr
  3. concentrationThe resulting mixture was concentrated under reduced pressure
  4. additiondiluted with H2O (50 mL)
  5. extractionextracted with EtOAc (100 mL)
  6. washwashed with H2O (100 mL)
  7. dry with materialdried (anhyd. Na2SO4)
  8. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-999f1fb3e4fe4b368a89d1f265e38c7e
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05646125

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