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Cyclohexyl isocyanide → HCID 178482102, 화합물

HRID 851756
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인쇄 미리보기

반응식

HRID 851756 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[CH:10][NH:11][CH:12]=2)=[CH:4][CH:3]=1.[CH:13]1([N+:19]#[C-:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>Cl[Cu]>[CH:13]1([NH:19][CH:20]=[N:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[N:9]=[CH:10][NH:11][CH:12]=3)=[CH:6][CH:7]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 79129Cyclohexyl isocyanideHCID 178507418HCID 178507418, 화합물

생성물 1

HCID 178482102HCID 178482102, 화합물

시약·촉매·용매 1

HCID 62652Cuprous chloride촉매

반응 조건

온도
150 °C

실험 절차

A mixture of 1.59 gm of 4-(p-aminophenyl)-1-H-imidazole, 1.2 gm of cyclohexyl isonitrile, and 0.99 gm of CuCl was heated at 150° C. for three hours. The thick reaction mixture was extracted with methanol. The methanol solution, after treatment with charcoal, was evaporated to dryness and extracted with ethyl acetate and 10% hydrochloric acid. The acid solution was adjusted to pH 7.5 with 17% Na2CO3 and extracted with ethyl acetate. The organic solution was evaporated to dryness. The substance remaining after recrystallization from acetone comprised 0.25 gm of the desired product.

후처리

  1. extractionThe thick reaction mixture was extracted with methanol
  2. customThe methanol solution, after treatment with charcoal, was evaporated to dryness
  3. extractionextracted with ethyl acetate and 10% hydrochloric acid
  4. extractionextracted with ethyl acetate
  5. customThe organic solution was evaporated to dryness
  6. customafter recrystallization from acetone

출처 및 근거

ORD 기록
ord-fa3d940e6f6e4aed9d190c9d3b878397
출처 데이터셋
uspto-grants-1983_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04386099

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