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1,1'-Carbonyldiimidazole → Ethyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate

HRID 1497668
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HRID 1497668 반응식
[C:1]([OH:7])(=[O:6])[CH2:2][C:3]([OH:5])=O.[CH2:8]([K])[CH3:9].[Mg+2].[Cl-].[Cl-].[F:14][C:15]1[C:16](C(O)=O)=[N:17][CH:18]=[CH:19][CH:20]=1.C(N1C=CN=C1)(N1C=CN=C1)=O>O1CCCC1.O>[CH2:8]([O:7][C:1](=[O:6])[CH2:2][C:3]([C:16]1[C:15]([F:14])=[CH:20][CH:19]=[CH:18][N:17]=1)=[O:5])[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 682631,1'-CarbonyldiimidazoleHCID 27627863-Fluoropyridine-2-carboxylic acidHCID 5360315Magnesium ChlorideHCID 178461627HCID 178461627, 화합물

생성물 1

HCID 59864622Ethyl 3-(3-fluoropyridin-2-yl)-3-oxopropanoate

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
2회

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온도
50 °C

실험 절차

To a solution of ethyl potassium malonate (2) (452 mg, 2.66 mmol) in tetrahydrofuran (5 mL) was added MgCl2 (202 mg, 2.13 mL). The mixture was stirred at 50° C. for 4 h and then cooled to room temperature. In another flask a solution of 3-fluoro-pyridine-2-carboxylic acid (1) (250 mg, 1.77 mmol) in tetrahydrofuran (5 mL) was taken and CDI (carbonyldiimidazole) (489 mg, 3.01 mmol) was added at 10° C. The mixture was stirred at room temperature for 1 h, this reaction mixture was then added to the above suspension and stirred at room temperature for 18 h. After completion of the reaction, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated.

후처리

  1. temperaturecooled to room temperature
  2. stirringThe mixture was stirred at room temperature for 1 h
  3. additionthis reaction mixture was then added to the above suspension
  4. stirringstirred at room temperature for 18 h
  5. additionwas added
  6. extractionthe mixture was extracted with ethyl acetate
  7. washThe organic layer was washed with brine
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0fbbb22fccd4481b8eaf2fb12366883b
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199987B2

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