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Trichloroacetonitrile → 2-(trichloromethyl)-1H-imidazole

HRID 869483
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HRID 869483 반응식
[Cl:1][C:2]([Cl:6])([Cl:5])[C:3]#[N:4].CO[CH:9](OC)[CH2:10][NH2:11]>C1COCC1>[Cl:1][C:2]([Cl:6])([Cl:5])[C:3]1[NH:11][CH:10]=[CH:9][N:4]=1
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참가 물질

4

반응물 2

HCID 11011TrichloroacetonitrileHCID 89728Aminoacetaldehyde dimethyl acetal

생성물 1

HCID 100811212-(trichloromethyl)-1H-imidazole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of trichloroacetonitrile (28.8 g, 200 mmol, 1 eq) in anhydrous THF (70 mL) at −60° C. under an argon atmosphere, 2,2-dimethoxyethanamine (21.8 mL, 200 mmol, 1.0 eq) was added dropwise over 5 min. The resulting mixture was allowed to warm to RT and stirred at RT for 4 h. The mixture was concentrated in vacuo and the residue was added in portions to a stirred solution of trifluoroacetic acid (100 mL) at −30° C. under argon. The resulting mixture was then stirred from −30° C. to RT overnight. The reaction mixture was concentrated in vacuo to afford 2-(trichloromethyl)-1H-imidazole. The crude product was used in the next step without further purification.

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. additionthe residue was added in portions to a stirred solution of trifluoroacetic acid (100 mL) at −30° C. under argon
  3. stirringThe resulting mixture was then stirred from −30° C. to RT overnight
  4. concentrationThe reaction mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-8d82c0590ad54cb985e5558a3e2e74ae
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969363B2

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