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Acetone → 1-[3-(Trifluoromethyl)phenyl]but-1-en-3-one

HRID 567129
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HRID 567129 반응식
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=O.[OH-].[Na+].O.C(OCC)(=O)C.[CH3:22][C:23]([CH3:25])=[O:24]>>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[C:5]([CH:6]=[CH:22][C:23](=[O:24])[CH3:25])[CH:8]=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 180AcetoneHCID 962WaterHCID 8857Ethyl AcetateHCID 14798Sodium HydroxideHCID 679903-(Trifluoromethyl)benzaldehyde

생성물 1

HCID 1449341-[3-(Trifluoromethyl)phenyl]but-1-en-3-one수율 88.7%

실험 절차

In a 250 ml single neck flask was charged 7.5 g (43.1 mmoles,1.0 eq) of m-trifluoromethylbenzaldehyde dissolved in 15 ml of acetone. To this was added 17.2 g of 10% aqueous sodium hydroxide solution (43 mmoles, 1.0 eq), dropwise and during the course of addition, temperature was kept no higher than 25° C., while the mixture was agitated continuously for 30 minutes. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to obtain 9.5 g of 4-(3-trifluoromethylphenyl)-3-buten-2-one as a faintly yellow oil in 88.7% yield.

후처리

  1. additiondropwise and during the course of addition, temperature
  2. customwas kept no higher than 25° C., while the mixture
  3. customthe phases were separated
  4. washthe organic phase was washed with water three times
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8d997b04a129467db86cf4a8b5980307
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06177462B1

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