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Methylamine → HCID 9795805, 화합물

HRID 376040
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HRID 376040 반응식
C[O:2][C:3](=O)/[C:4](/[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=1)=[N:5]/[OH:6].[CH3:22][NH2:23]>CO>[OH:6]/[N:5]=[C:4](\[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=1)/[C:3]([NH:23][CH3:22])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329Methylamine2회HCID 88361076HCID 88361076, 화합물

생성물 1

HCID 9795805HCID 9795805, 화합물수율 100%

시약·촉매·용매 1

HCID 887Methanol용매3회

실험 절차

E-α-hydroxyimino-2-(4-methylphenoxy)phenylacetic acid methyl ester (1.00 g, 0.0035 mole) was dissolved in methanol (7 ml) and 40% methylamine solution in methanol (0.54 g, 0,007 mole) was added to the mixture, which was refluxed for 70 minutes. A 40% methylamine solution in methanol (1.36 g, 0.0175 mole) was further added to the mixture, which was refluxed for 3 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure to give E-2-hydroxyimino-N-methyl-2-[2-(4methylphenoxy)phenyl]acetamide (1.00 g, yield: 100.0 %) as an amorphous.

후처리

  1. temperaturewas refluxed for 70 minutes
  2. temperaturewas refluxed for 3 hours
  3. customAfter completion of the reaction
  4. concentrationthe reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f349e3d194634951930b59a45ab6212d
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05488159

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