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Tetrahydrofuran → 1-[1-(3,4-dichloro-phenyl)-1H-imidazol-4-yl]-ethanol

HRID 1841221
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HRID 1841221 반응식
C[Mg]I.[Cl:4][C:5]1[CH:6]=[C:7]([N:12]2[CH:16]=[C:15]([CH:17]=[O:18])[N:14]=[CH:13]2)[CH:8]=[CH:9][C:10]=1[Cl:11].[CH2:19]1COCC1.[Cl-].[NH4+]>CCOCC>[Cl:4][C:5]1[CH:6]=[C:7]([N:12]2[CH:16]=[C:15]([CH:17]([OH:18])[CH3:19])[N:14]=[CH:13]2)[CH:8]=[CH:9][C:10]=1[Cl:11]
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참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 234451021-(3,4-dichloro-phenyl)-1H-imidazole-4-carbaldehydeHCID 178418373HCID 178418373, 화합물

생성물 1

HCID 234449581-[1-(3,4-dichloro-phenyl)-1H-imidazol-4-yl]-ethanol수율 93%

시약·촉매·용매 1

HCID 3283
Diethyl Ether
용매
2회

실험 절차

To a solution of methylmagnesium iodide in ether (3 M, 13,7 ml, 41.1 mmol) and ether (40 ml), 1-(3,4-dichloro-phenyl)-1H-imidazole-4-carbaldehyde (2.58 g, 10.7 mmol) was added in portions. THF (50 ml) was then added slowly and stirring was continued for 1 h at reflux. After the addition of aqueous ammonium chloride (saturated, 30 ml), the mixture was extracted with AcOEt. The organic phase was dried (Na2SO4) and evaporated to give 1-[1-(3,4-dichloro-phenyl)-1H-imidazol-4-yl]-ethanol (2.56 g, 93%) as a light brown solid. MS: m/e=257.0 (M+H+).

후처리

  1. temperatureat reflux
  2. extractionthe mixture was extracted with AcOEt
  3. dry with materialThe organic phase was dried (Na2SO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-4ab69b4317b9432c8161ba24cbfff142
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06683097B2

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