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Perfluoro-1-butanesulfonyl fluoride → 2-Pyrazinecarboxylic acid, 5-(fluoromethyl)-, methyl ester

HRID 2045857
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HRID 2045857 반응식
O[CH2:2][C:3]1[N:4]=[CH:5][C:6]([C:9]([O:11][CH3:12])=[O:10])=[N:7][CH:8]=1.F.F.F.C(N(CC)CC)C.[F:23]C(F)(C(F)(F)F)C(F)(F)C(F)(F)S(F)(=O)=O.C([O-])(O)=O.[Na+]>C1COCC1.C(N(CC)CC)C>[F:23][CH2:2][C:3]1[N:4]=[CH:5][C:6]([C:9]([O:11][CH3:12])=[O:10])=[N:7][CH:8]=1
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참가 물질

7

반응물 4

HCID 67814Perfluoro-1-butanesulfonyl fluorideHCID 175505N,N-Diethylethanamine trihydrofluorideHCID 516892Sodium BicarbonateHCID 66869530Methyl 5-(hydroxymethyl)pyrazine-2-carboxylate

생성물 1

HCID 699365032-Pyrazinecarboxylic acid, 5-(fluoromethyl)-, methyl ester수율 14.5%

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
HCID 8471Triethylamine용매

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온도
0 °C

실험 절차

To a solution of methyl 5-(hydroxymethyl)pyrazine-2-carboxylate (0.64 g) in THF (20 mL) was added triethylamine (2.30 g) and the solution was cooled to 0° C. Triethylamine trihydrofluoride (1.22 g) was then added followed by nonafluorobutanesulfonyl fluoride (2.28 g) dropwise over 5 mins. After warming to RT and stirring for 2 h, NaHCO3 (sat., aq., 100 mL) was added, and the mixture was extracted with EtOAc (2×50 mL). The combined organic portions were dried over MgSO4, evaporated, and purified by silica gel chromatography (5% to 50% EtOAc in hexane) to afford the title compound (94 mg). 1H NMR (400 MHz, CDCl3) δ ppm 4.07 (s, 3H), 5.67 (d, J=46.5 Hz, 2H), 8.89 (s, 1H), 9.28 (s, 1H)

후처리

  1. temperatureAfter warming to RT
  2. extractionthe mixture was extracted with EtOAc (2×50 mL)
  3. dry with materialThe combined organic portions were dried over MgSO4
  4. customevaporated
  5. custompurified by silica gel chromatography (5% to 50% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-1b49d2d543ff45e2a64ac3ddeca22de7
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592408B2

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