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Dimethylformamide → 2-Furancarboxaldehyde, 5-(3,4-dimethoxyphenyl)-, O-[(methylamino)carbonyl]oxime

HRID 1759148
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반응식

HRID 1759148 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[O:15][C:14]([CH:16]=[N:17][OH:18])=[CH:13][CH:12]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[CH3:19][N:20]([CH:22]=[O:23])C.CN=C=O>O>[CH3:19][NH:20][C:22]([O:18][N:17]=[CH:16][C:14]1[O:15][C:11]([C:5]2[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)=[CH:12][CH:13]=1)=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 12228Methyl IsocyanateHCID 71382179N-{[5-(3,4-Dimethoxyphenyl)furan-2-yl]methylidene}hydroxylamine

생성물 1

HCID 540343162-Furancarboxaldehyde, 5-(3,4-dimethoxyphenyl)-, O-[(methylamino)carbonyl]oxime수율 51%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-(3,4-Dimethoxyphenyl)furylformaldoxime (9.5 g, 0.038 mole) and DMF (500 ml) was treated with methyl isocyanate (16 ml, 0.27 mole). The solution was stirred at room temperature for 4 hours and at steam bath temperature for 1 hour. The reaction solution was poured into 3 liters of water. The tan precipitate was collected to give 6 g (51%) of product.

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후처리

  1. customThe tan precipitate was collected

출처 및 근거

ORD 기록
ord-82648de394dd45e3bbedeb24bc1918e0
출처 데이터셋
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04339386

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