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Vanillin → 4-(allyloxy)-3-methoxybenzaldehyde

HRID 746328
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HRID 746328 반응식
[O:1]=[CH:2][C:3]1[CH:11]=[CH:10][C:8]([OH:9])=[C:5]([O:6][CH3:7])[CH:4]=1.[CH2:12](Br)[CH:13]=[CH2:14].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:7][O:6][C:5]1[CH:4]=[C:3]([CH:11]=[CH:10][C:8]=1[O:9][CH2:14][CH:13]=[CH2:12])[CH:2]=[O:1]
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참가 물질

5

반응물 3

HCID 1183VanillinHCID 7841Allyl bromideHCID 11430Potassium Carbonate

생성물 1

HCID 20638234-(allyloxy)-3-methoxybenzaldehyde

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Vanillin (20.0 g, 0.130 mol) and allyl bromide (19.9 g, 0.160 mol) were heated under reflux together with potassium carbonate (27.3 g, 0.200 mol) in 150 ml acetone (abs.) for 8 hours. After cooling, the solid was filtered off and washed with acetone. A yellow oil was obtained after a thorough concentration of the organic phases.

후처리

  1. temperatureAfter cooling
  2. filtrationthe solid was filtered off
  3. washwashed with acetone
  4. customA yellow oil was obtained
  5. concentrationafter a thorough concentration of the organic phases

출처 및 근거

ORD 기록
ord-2262e4da654c4dfa925ae01a12cfcfdc
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07393367B2

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