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Imidazole → 1-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole

HRID 463280
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HRID 463280 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[C:6]([C:10]1[CH:15]=[CH:14][C:13]([C:16](=[O:21])[CH2:17][CH2:18][CH2:19]Cl)=[CH:12][CH:11]=1)([CH3:9])([CH3:8])[CH3:7]>CN(C)C=O>[C:6]([C:10]1[CH:11]=[CH:12][C:13]([C:16](=[O:21])[CH2:17][CH2:18][CH2:19][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)=[CH:14][CH:15]=1)([CH3:9])([CH3:8])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 795ImidazoleHCID 27236944'-tert-Butyl-4-chlorobutyrophenone

생성물 1

HCID 202824961-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole수율 80.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a 0° C. slurry of 8.24 g of imidazole in 15 ml. dry dimethylformamide was added 5.79 g of p-t-butyl-gamma-chlorobutyrophenone and the mixture was stirred overnight at room temperature, then for one day at 60° C. The above solution was poured into 400 ml. of water and extracted three times with ethyl acetate. The combined extracts were washed with water, dried over magnesium sulfate and the solvent evaporated to afford 5.25 g of 1-[4-(4-t-butylphenyl)butan-4-onyl]imidazole as a golden oil.

후처리

  1. customTo a 0° C.
  2. waitfor one day at 60° C
  3. additionThe above solution was poured into 400 ml
  4. extractionof water and extracted three times with ethyl acetate
  5. washThe combined extracts were washed with water
  6. dry with materialdried over magnesium sulfate
  7. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-5474642cacfe4a3b81f6d870e9488a59
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04518607

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