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Acetanilide → HCID 21998426, 화합물

HRID 1976520
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HRID 1976520 반응식
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)(=O)[CH3:2].[C:11](=[O:14])([O-])[O-:12].[K+].[K+].[OH-].[K+]>S([O-])([O-])(=O)=O.[Cu+2].CO>[CH2:11]1[O:14][C:6]2[CH:5]=[CH:10][C:1]([NH:4][C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=3)=[CH:2][C:7]=2[O:12]1
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참가 물질

6

반응물 3

HCID 904AcetanilideHCID 11430Potassium CarbonateHCID 14797Potassium Hydroxide

생성물 1

HCID 21998426HCID 21998426, 화합물수율 167.1%

시약·촉매·용매 2

HCID 24462Copper Sulfate촉매HCID 887Methanol용매

실험 절차

A mixture of 90 g (0.448 mol) of 3,4-bromomethylenedioxybenzene, 50 g (0.37 mol) of acetanilide, 12 g (0.075 mol) of copper sulfate, and 80 g (0.579 mol) of potassium carbonate was reacted in the same manner as in Example 5 (2) to obtain a crude reaction product. A mixture of this crude product, 121.4 g (1.84 mol) of 85% KOH, and 200 ml of methanol was refluxed overnight and then concentrated. Water was added thereto. The resultant mixture was extracted with toluene twice. The toluene phase was washed with water three times, dried, and then concentrated. The residue was distilled under vacuum to obtain 65.91 g of N-3,4-methylenedioxyphenyl-N-phenylamine.

후처리

  1. customto obtain a crude
  2. customreaction product
  3. temperaturewas refluxed overnight
  4. concentrationconcentrated
  5. additionWater was added
  6. extractionThe resultant mixture was extracted with toluene twice
  7. washThe toluene phase was washed with water three times
  8. customdried
  9. concentrationconcentrated
  10. distillationThe residue was distilled under vacuum

출처 및 근거

ORD 기록
ord-98fe596881c64463b5ab0a7d67c397a3
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06228547B1

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