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Water → 4-Methoxy-3-(methoxymethoxy)benzaldehyde

HRID 2254209
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HRID 2254209 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[O:10])=[CH:5][C:4]=1[OH:11].C(N(CC)C(C)C)(C)C.[CH3:21][O:22][CH2:23]Cl.O>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[O:10])=[CH:5][C:4]=1[O:11][CH2:21][O:22][CH3:23]
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참가 물질

6

반응물 4

HCID 962WaterHCID 7864Chloromethyl Methyl EtherHCID 12127IsovanillinHCID 81531Diisopropylethylamine

생성물 1

HCID 6401524-Methoxy-3-(methoxymethoxy)benzaldehyde수율 85%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

In 100 ml of dimethylformamide was dissolved 10 g of isovaniline, and 14 ml of N,N-diisopropylethylamine was added to the solution and the mixture was stirred. The liquid mixture was cooled to 0° C. and 7.2 ml of chloromethyl methyl ether was added to the mixture, and the temperature was elevated to room temperature and the mixture was stirred for 5 hours. After the reaction, a large quantity of water was added to the reaction mixture, and the mixture was extracted with diethyl ether, washed with water and dried. Removal of the solvent by distillation gave 11.0 g (yield=85%) of 4-methoxy-3-methoxymethoxybenzaldehyde in the form of a yellow oil.

후처리

  1. additionwas added to the solution
  2. customwas elevated to room temperature
  3. stirringthe mixture was stirred for 5 hours
  4. customAfter the reaction
  5. extractionthe mixture was extracted with diethyl ether
  6. washwashed with water
  7. customdried
  8. customRemoval of the solvent
  9. distillationby distillation

출처 및 근거

ORD 기록
ord-3126b14c96df4c37936ec2ccc7a379a3
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05234951

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