Sulfuryl chloride → Ethyl 3-chloro-2-oxopiperidine-3-carboxylate

HRID 1398199Notes

Reaction equation

HRID 1398199 reaction equation
[O:1]=[C:2]1[CH:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:6][CH2:5][CH2:4][NH:3]1.S(Cl)([Cl:16])(=O)=O.C(=O)([O-])O.[Na+]>C1COCC1>[Cl:16][C:7]1([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:6][CH2:5][CH2:4][NH:3][C:2]1=[O:1]

Participants

5

Procedure

To a mixture of ethyl 2-oxopiperidine-3-carboxylate (30 g) in THF (300 mL) was added dropwise sulfuryl chloride (14.2 mL) at 0° C-5° C., and the mixture was stirred at room temperature for 18 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution (300 mL) at 0° C., and the mixture was stirred at room temperature for 30 min and extracted with ethyl acetate (300 mL×3). The extract was washed with saturated brine (300 mL), and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with hexane/ethyl acetate (5/1, 60 mL×2) to give the title compound (32.7 g).

Workup

  1. stirringthe mixture was stirred at room temperature for 30 min
  2. extractionextracted with ethyl acetate (300 mL×3)
  3. washThe extract was washed with saturated brine (300 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. washThe residue was washed with hexane/ethyl acetate (5/1, 60 mL×2)

Sources & evidence

ORD record
ord-96a2a23957d64f3d8ae5c1875c7c0dd2
Source dataset
uspto-grants-2014_12
Patent number
US08901309B2

Reaction notes

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