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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 1463484-29-8

HRID 338067
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HRID 338067 반응식
[F:1][C:2]1[CH:3]=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[C:9](OOC(=O)C1C=CC=CC=1)(=[O:16])C1C=CC=CC=1.FC(F)(F)C(O)=O>CO>[Cl:8][C:5]1[N:6]=[C:7]([CH2:9][OH:16])[C:2]([F:1])=[CH:3][N:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 7187Benzoyl PeroxideHCID 5834662-Chloro-5-fluoropyrimidine

생성물 1

HCID 866978861463484-29-8수율 25%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
65 °C

실험 절차

To a solution of 5-fluoro-2-chloropyrimidine (500 μL, 5.24 mmol) in methanol (50 mL) is added benzoyl peroxide (1.5 g, 6.0 mmol) and trifluoroacetic acid (450 μL, 5.95 mmol). The resulting colorless clear solution is degassed by bubbling nitrogen through for 5 minutes and it is then heated at 65° C. for 18.5 hours. The solution is then cooled and concentrated. The resulting residue is diluted with chloroform (50 mL) and washed with saturated aqueous sodium bicarbonate solution (50 mL) and the layers are separated. The aqueous layer is re-extracted with chloroform (50 mL). The combined organic layers are dried over magnesium sulfate, filtered and concentrated to dryness under reduced vacuum. The residue is purified by flash silica gel column chromatography, eluting with gradient of ethyl acetate/dichloromethane (0% to 30%) to give the title compound (210 mg, 25%). 1H-NMR (CDCl3): δ (ppm) 8.42 (s, 1H), 4.85 (s, 2H), 3.57 (br, 1H).

후처리

  1. customThe resulting colorless clear solution is degassed
  2. customby bubbling nitrogen through for 5 minutes and it
  3. temperatureThe solution is then cooled
  4. concentrationconcentrated
  5. additionThe resulting residue is diluted with chloroform (50 mL)
  6. washwashed with saturated aqueous sodium bicarbonate solution (50 mL)
  7. customthe layers are separated
  8. extractionThe aqueous layer is re-extracted with chloroform (50 mL)
  9. dry with materialThe combined organic layers are dried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated to dryness under reduced vacuum
  12. customThe residue is purified by flash silica gel column chromatography
  13. washeluting with gradient of ethyl acetate/dichloromethane (0% to 30%)

출처 및 근거

ORD 기록
ord-967f3604e010462c856c5a39b113e2b8
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889856B2

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