Reaktion #5573

ord-000317cc53274835920257e50a875bf5

Reaktionsgleichung

OC1CCNCC1
4-hydroxypiperidine
CCN(CC)CC
triethylamine
CS(=O)(=O)Cl
methanesulfonyl chloride
CS(=O)(=O)OC1CCN(S(C)(=O)=O)CC1
desired product
Ausbeute 89.0%
CS(=O)(=O)OC1CCN(S(C)(=O)=O)CC1
1-methylsulfonyl-4-methylsulfonyloxypiperidine
Ausbeute 89.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hour
  3. 3
    WaschenThe reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline
  4. 4
    Trocknendried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONAfter the solvent was distilled off

Vorschrift

To a solution of 4-hydroxypiperidine (5.10 g, 50 mmoles) and triethylamine (20.9 ml, 150 mmoles) in methylene chloride (150 ml) was added methanesulfonyl chloride (8.54 ml, 110 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was solidified with ethyl acetate-n-hexane to obtain 11.45 g of the desired product (88.3%, pale yellow solid).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244908uspto-grants-1993_09