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Dimethylformamide → Methyl 3-acetyl-4-methoxybenzoate

HRID 1003354
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HRID 1003354 반응식
[C:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1O)[C:7]([OH:9])=[O:8])(=[O:3])[CH3:2].CI.[C:16](=O)([O-])[O-].[K+].[K+].CN([CH:25]=[O:26])C>>[C:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[O:26][CH3:25])[C:7]([O:9][CH3:16])=[O:8])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 91792453-Acetyl-4-hydroxybenzoic acid

생성물 1

HCID 10798398Methyl 3-acetyl-4-methoxybenzoate

실험 절차

3-Acetyl-4-hydroxybenzoic acid (3.60 g, 20 mmol) and methyl iodide (5.68 g, 40 mmol) were dissolved in 60 ml of DMF, followed by the addition of 11.06 g (80 mmol) of potassium carbonate. The resulting mixture was stirred at room temperature for 2 hours. The DMF was distilled off under reduced pressure, followed by the addition of water. The resulting mixture was extracted with chloroform. The organic layer was dried over MgSO4, the solvent was distilled off under reduced pressure, and the residue was recrystallized from acetone-hexane, whereby 1.42 g of the title compound were obtained as brown powder (yield: 34%).

후처리

  1. distillationThe DMF was distilled off under reduced pressure
  2. additionfollowed by the addition of water
  3. extractionThe resulting mixture was extracted with chloroform
  4. dry with materialThe organic layer was dried over MgSO4
  5. distillationthe solvent was distilled off under reduced pressure
  6. customthe residue was recrystallized from acetone-hexane

출처 및 근거

ORD 기록
ord-0babf8cb5bcb46ebbe683ced8c096fac
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046212

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