Pyridine → HCID 19860691, Verbindung

HRID 2309602Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2309602
[F:1][C:2]([F:8])([CH2:5][CH2:6][OH:7])[CH2:3][OH:4].N1C=CC=CC=1.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>ClCCl>[CH3:15][S:16]([O:4][CH2:3][C:2]([F:8])([F:1])[CH2:5][CH2:6][O:7][S:16]([CH3:15])(=[O:18])=[O:17])(=[O:18])=[O:17]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 31297Methanesulfonyl chlorideHCID 13935577108781-20-0

Produkt 1

HCID 19860691HCID 19860691, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a stirred mixture of 2,2-difluoro-1,4-butanediol (12.97 g, 103 mM), dry pyridine (65 mL) and dichloromethane (200 mL) is slowly added a solution of methanesulfonylchloride (23.6 g) in dichloromethane (50 mL). Stirring is continued overnight. The reaction mixture is washed with 2N HCl (twice), followed by 10% aqueous NaHCl3 until neutral, and then with water. The organic layer is dried (MgSO4) and upon evaporation of the solvents, a slightly yellow oil is obtained. Crystallization is induced by scratching the oil with dry ether, to yield the compound 1,4-bis-methanesulfonyloxy-2,2-difluorobutane as white crystals: 22.3 g (77%).

Aufarbeitung

  1. washThe reaction mixture is washed with 2N HCl (twice),
  2. dry with materialThe organic layer is dried (MgSO4)
  3. customupon evaporation of the solvents
  4. customa slightly yellow oil is obtained
  5. customCrystallization

Quellen und Nachweise

ORD-Eintrag
ord-a3a87ca60e45496caee606dd80eb05d4
Quelldatensatz
uspto-grants-1987_09
Patentnummer
US04695654

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