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Vanillin → 3-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde

HRID 1951967
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HRID 1951967 반응식
C(=O)([O-])[O-].[K+].[K+].Cl[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1.[OH:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=[O:23])=[CH:20][C:19]=1[O:26][CH3:27]>CC(C)=O.CCCCCCC>[CH3:27][O:26][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][C:18]=1[O:17][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1)[CH:22]=[O:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 1183VanillinHCID 11430Potassium CarbonateHCID 699934-Methyloxybenzyl chloride

생성물 1

HCID 27644923-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde수율 100%

시약·촉매·용매 2

HCID 180Acetone용매HCID 8900Heptane용매

반응 조건

온도
55 °C

실험 절차

5 g (36.1 mmol) of potassium carbonate and then 4.9 ml (36.1 mmol) of 1-chloromethyl-4-methoxy-benzene are added to a solution of 5 g (33 mmol) of 4-hydroxy-3-methoxy-benzaldehyde in 100 ml of acetone. The reaction mixture is then stirred at 55° C. for 28 hours and then filtered. The filtrate is concentrated under vacuum. The residue obtained is taken up in heptane and filtered. 8.9 g (100%) of 3-methoxy-4-(4-methoxy-benzyloxy)-benzaldehyde is obtained in the form of a beige solid.

후처리

  1. filtrationfiltered
  2. concentrationThe filtrate is concentrated under vacuum
  3. customThe residue obtained
  4. filtrationfiltered

출처 및 근거

ORD 기록
ord-43fe7caa76d942678f269dbe2dedd8f9
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08404836B2

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