Sodium Sulfite → 5-Bromo-2-(((fluoromethyl)sulfonyl)methyl)pyridine

HRID 1500294Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1500294
[F:1][CH2:2][S:3](Cl)(=[O:5])=[O:4].S([O-])([O-])=O.[Na+].[Na+].C(=O)(O)[O-].[Na+].[Br:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25]Cl)=[N:23][CH:24]=1>O.C(O)C>[Br:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][S:3]([CH2:2][F:1])(=[O:5])=[O:4])=[N:23][CH:24]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Commercially available fluoromethanesulfonyl chloride (975 mg, 7.36 mmol) is added dropwise to a solution of sodium sulfite (1.85 g, 14.7 mmol) and sodium bicarbonate (1.24 g, 14.7 mmol) in water (2 mL). The reaction mixture is heated in a microwave reactor to 100° C. for 20 minutes. After cooling to room temperature commercially available 5-bromo-2-(chloromethyl)pyridine (894 mg, 3.68 mmol) in ethanol (2 mL) is added. The mixture is heated in a microwave reactor to 100° C. for 20 minutes. The reaction mixture is cooled to 0° C. and the solid filtered off and discarded. The filtrates are diluted with saturated sodium carbonate (10 mL), extracted with tertiarybutyl methyl ether (50 mL). The organic layer is separated, dried over sodium sulfate, filtered and the solvent removed under reduced pressure to give the title compound (150 mg): m/z 268.9 (M+H)+.

Aufarbeitung

  1. additionis added
  2. temperatureThe mixture is heated in a microwave reactor to 100° C. for 20 minutes
  3. temperatureThe reaction mixture is cooled to 0° C.
  4. filtrationthe solid filtered off
  5. additionThe filtrates are diluted with saturated sodium carbonate (10 mL)
  6. extractionextracted with tertiarybutyl methyl ether (50 mL)
  7. customThe organic layer is separated
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. customthe solvent removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f82baee5382e4004a99c8ca3ae5ebdd4
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09206126B2

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