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Mesitylene → 3-Allyl-4-hydroxy-5-methoxy-benzaldehyde

HRID 746329
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HRID 746329 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11]CC=C)[CH:6]=[O:7].[OH-].[Na+].[C:17]1(C)[CH:22]=C(C)C=C(C)[CH:18]=1>>[CH2:22]([C:9]1[CH:8]=[C:5]([CH:4]=[C:3]([O:2][CH3:1])[C:10]=1[OH:11])[CH:6]=[O:7])[CH:17]=[CH2:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7947MesityleneHCID 14798Sodium HydroxideHCID 20638234-(allyloxy)-3-methoxybenzaldehyde

생성물 1

HCID 15338063-Allyl-4-hydroxy-5-methoxy-benzaldehyde

실험 절차

3-Methoxy-4-(2-propenyloxy)benzaldehyde (19.7 g, 0.100 mol) was heated under reflux in 75 ml mesitylene (1,3,5-trimethylbenzene) for 20 hours. After cooling, 250 ml 2N sodium hydroxide were added to the reaction mixture. The aqueous phase was washed two times with diethyl ether. The aqueous phase was subsequently acidified with concentrated hydrochloric acid under ice cooling and then extracted with ethyl acetate. After drying and concentrating the organic phase, there remained a light orange-colored oil that crystallized on cooling.

후처리

  1. temperatureAfter cooling
  2. washThe aqueous phase was washed two times with diethyl ether
  3. extractionextracted with ethyl acetate
  4. customAfter drying
  5. concentrationconcentrating the organic phase, there
  6. customthat crystallized
  7. temperatureon cooling

출처 및 근거

ORD 기록
ord-a85e475e5a284b7cb732c9fb8d9f8aa3
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07393367B2

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