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Acetone → (E)-4-(3-fluorophenyl)but-3-en-2-one

HRID 1189547
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HRID 1189547 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.[CH3:10][C:11]([CH3:13])=[O:12].[OH-].[Na+]>O>[F:1][C:2]1[CH:3]=[C:4](/[CH:5]=[CH:10]/[C:11](=[O:12])[CH3:13])[CH:7]=[CH:8][CH:9]=1
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 680093-Fluorobenzaldehyde

생성물 1

HCID 23269545(E)-4-(3-fluorophenyl)but-3-en-2-one수율 112%

시약·촉매·용매 1

HCID 962Water용매

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온도
65 °C

실험 절차

To a mixture of 3-fluorobenzaldehyde (4.0 ml, 37.7 mmol) and acetone (8.86 ml, 121 mmol) in water (10 ml), was added 0.25 M sodium hydroxide (15.08 ml, 3.77 mmol). The reaction mixture was heated at 65° C. for 2 h. The mixture was poured into ice water and extracted with ethyl acetate (200 ml). The organic layer was dried, filtered, and evaporated to give (E)-4-(3-fluorophenyl)but-3-en-2-one as yellow oil. It was used for the next reaction without purification (6.92 g, 42.1 mmol, 112% yield). 1H NMR (CDCl3/400 MHz): δ (ppm) 7.46 (d, 1H), 7.40-7.34 (m, 1H), 7.33-7.29 (m, 1H), 7.26-7.21 (m, 1H), 7.12-7.06 (m, 1H), 6.70 (d, 1H), 2.38 (s, 3H).

후처리

  1. extractionextracted with ethyl acetate (200 ml)
  2. customThe organic layer was dried
  3. filtrationfiltered
  4. customevaporated

출처 및 근거

ORD 기록
ord-7befdcc2e90b49e2a2643972af795cee
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08674115B2

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