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Sodium Carbonate → 3-Allyl-4-hydroxybenzamidoxime

HRID 861427
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인쇄 미리보기

반응식

HRID 861427 반응식
[CH2:1]([C:4]1[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[CH:6][C:5]=1[OH:12])[CH:2]=[CH2:3].Cl.[NH2:14][OH:15].C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH2:1]([C:4]1[CH:9]=[C:8]([CH:7]=[CH:6][C:5]=1[OH:12])[C:10](=[N:14][OH:15])[NH2:11])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 2584423-Allyl-4-hydroxybenzonitrileHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 1360876093-Allyl-4-hydroxybenzamidoxime수율 82.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-allyl-4-cyanophenol (5.5 g), hydroxylamine hydrochloride (8.5 g) and sodium carbonate (6.1 g) in aqueous ethanol was heated at reflux for 3 hours. The solution was cooled to ambient temperature and the ethanol was removed by evaporation. The solid was collected by filtration, dissolved in ethanol and the solution was filtered. The filtrate was evaporated and the residual solid was triturated with hexane to give 3-allyl-4-hydroxybenzamidoxime as a solid (5.5 g), m.p. 144° C.

후처리

  1. temperatureat reflux for 3 hours
  2. customthe ethanol was removed by evaporation
  3. filtrationThe solid was collected by filtration
  4. dissolutiondissolved in ethanol
  5. filtrationthe solution was filtered
  6. customThe filtrate was evaporated
  7. customthe residual solid was triturated with hexane

출처 및 근거

ORD 기록
ord-fa68b737bee540c3a23ea665129b0621
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05714496

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