Dimethyl Sulfoxide → Tert-butyl 3-oxopiperidine-1-carboxylate

HRID 1611910Notes

Reaction equation

HRID 1611910 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[C:11]([O:15][C:16]([N:18]1[CH2:23][CH2:22][CH2:21][CH:20]([OH:24])[CH2:19]1)=[O:17])([CH3:14])([CH3:13])[CH3:12].C(N(CC)CC)C>C(Cl)Cl.O>[C:11]([O:15][C:16]([N:18]1[CH2:23][CH2:22][CH2:21][C:20](=[O:24])[CH2:19]1)=[O:17])([CH3:14])([CH3:12])[CH3:13]

Participants

7

Conditions

Temperature
-78 °C

Procedure

A mixture of DMSO (7.8 mL, 109.3 mmol) and methylene chloride (100 mL) was cooled to −78° C. Oxalyl chloride (4.8 mL, 54.7 mmol) was added to this solution via syringe. The mixture was stirred at −78° C. for 30 min. A solution of 3-hydroxypiperidine-1-carboxylic acid tert-butyl ester (10.0 g, 49.7 mmol) in methylene chloride (30 mL) was added dropwise to this solution (temperature remained below −70° C.). The mixture was stirred for 30 min. Triethylamine (28 mL, 200 mmol) was added dropwise over 20 min. The mixture was stirred at −78° C. for 1 h and was allowed to warm to room temperature and stirred for 45 min. The mixture was diluted with water, and the layers separated. The organic layer was washed with water, dried Na2SO4), filtered, and concentrated to give 3-oxopiperidine-1-carboxylic acid tert-butyl ester (10.2 g) as a yellow, brown liquid.

Workup

  1. stirringThe mixture was stirred for 30 min
  2. stirringThe mixture was stirred at −78° C. for 1 h
  3. temperatureto warm to room temperature
  4. stirringstirred for 45 min
  5. customthe layers separated
  6. washThe organic layer was washed with water, dried Na2SO4),
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-beda330daffa4deb8939c3eeec293710
Source dataset
uspto-grants-2006_01
Patent number
US06992082B2

Reaction notes

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