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Water → HCID 73668580, 화합물

HRID 1450448
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HRID 1450448 반응식
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:7][C:4]=1[CH:5]=O.[OH2:18].Cl.[NH2:20]O.C([O-])(=O)C.[Na+]>CO>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:7][C:4]=1[CH:5]=[N:20][OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 199760832-Methoxy-5-phenoxybenzaldehyde

생성물 1

HCID 73668580HCID 73668580, 화합물수율 98%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

2-Methoxy-5-phenoxybenzaldehyde (4.5 g, 19.7 mmol) was dissolved in 60 ml of warm methanol. Water (40 ml) was added to this solution followed by the addition of hydroxylamine hydrochloride (2.7 g, 38.9 mmol) and anhydrous sodium acetate (6.5 g, 79.2 mmol). This mixture was then refluxed for 4 hours. The reaction mixture was concentrated under reduced pressure to remove the methanol. The residue was partitioned with ethyl acetate. The ethyl acetate layer was separated, washed five times with water, dried (anhydrous MgSO4) and the solvent removed under reduced pressure to give 2-methoxy-5-phenoxybenzaldehyde oxime as a white crystalline solid (4.70 g, 98%), mp 95°-100° C.

후처리

  1. temperatureThis mixture was then refluxed for 4 hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customto remove the methanol
  4. customThe residue was partitioned with ethyl acetate
  5. customThe ethyl acetate layer was separated
  6. washwashed five times with water
  7. dry with materialdried (anhydrous MgSO4)
  8. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-5e7d981626b24b6a9909d64e21a0834b
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05602151

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