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2-Benzofurancarbonitrile, 4-methoxy- → 1-(Hydroxyimino)-1-(4-methoxybenzo(b)furan-2-yl)methylamine

HRID 460565
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반응식

HRID 460565 반응식
[CH3:1][O:2][C:3]1[C:11]2[CH:10]=[C:9]([C:12]#[N:13])[O:8][C:7]=2[CH:6]=[CH:5][CH:4]=1.Cl.[NH2:15][OH:16].C(=O)([O-])O.[Na+]>C(O)C>[OH:16][N:15]=[C:12]([NH2:13])[C:9]1[O:8][C:7]2[CH:6]=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[C:11]=2[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2152702-Benzofurancarbonitrile, 4-methoxy-HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium Bicarbonate

생성물 1

HCID 30694661-(Hydroxyimino)-1-(4-methoxybenzo(b)furan-2-yl)methylamine수율 102%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution (40 ml) of 4-methoxybenzo(b)furan-2-carbonitrile (2.8 g) in ethanol were added hydroxylamine hydrochloride (1.2 g) and sodium hydrogencarbonate (3.0 g). The mixture was refluxed under heating for 1.5 hr. The inorganic material was filtered off and the reaction mixture was concentrated under reduced pressure to give the title compound (3.4 g) as brown crystals.

후처리

  1. temperatureThe mixture was refluxed
  2. temperatureunder heating for 1.5 hr
  3. filtrationThe inorganic material was filtered off
  4. concentrationthe reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-db3723df7251483195991df12b590345
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07196199B2

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