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Ethanol → HCID 54226506, 화합물

HRID 1723116
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HRID 1723116 반응식
[N:1]1([CH:6]([C:8]2[CH:13]=[CH:12][C:11]([NH:14]C)=[C:10]([N+:16]([O-])=O)[CH:9]=2)[CH3:7])[CH:5]=[CH:4][N:3]=[CH:2]1.[H][H].[CH2:21](O)C>[Ni]>[N:1]1([CH:6]([C:8]2[CH:9]=[C:10]([NH:16][CH3:21])[C:11]([NH2:14])=[CH:12][CH:13]=2)[CH3:7])[CH:5]=[CH:4][N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 20026658HCID 20026658, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 54226506HCID 54226506, 화합물수율 100%

시약·촉매·용매 1

HCID 935Nickel촉매

실험 절차

(b-1) A mixture of 21 parts of 4-[1-(1H-imidazol-1-yl)ethyl]-N-methyl-2-nitrobenzenamine and 160 parts of ethanol was hydrogenated at room temperature in a Parr apparatus at 0.5 105Pa with 20 parts of Raney-nickel catalyst. After the calculated amount of hydrogen was taken up, nitrogen was bubbled through the mixture and the catalyst was filtered off over diatomaceous earth. The filtrate was evaporated at <40° C., yielding 18.5 parts (100%) of 4-[1-(1H-imidazol-1-yl)ethyl]-N2 -methyl-1,2-benzenediamine as a residue (int. 97).

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후처리

  1. customnitrogen was bubbled through the mixture
  2. filtrationthe catalyst was filtered off over diatomaceous earth
  3. customThe filtrate was evaporated at <40° C.

출처 및 근거

ORD 기록
ord-a83ee54bc022405f9734b65d9a05caad
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04859684

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