Dimethylformamide → 57805-14-8

HRID 591058Notes

Reaction equation

HRID 591058 reaction equation
[CH3:1][N:2]([CH3:5])[CH:3]=[O:4].CN1[C:11](=[O:12])[CH2:10][S:9]C1=O.P(Cl)(Cl)([Cl:16])=O>>[Cl:16][C:1]1[N:2]([CH3:5])[C:3](=[O:4])[S:9][C:10]=1[CH:11]=[O:12]

Participants

4

Conditions

Temperature
110 °C

Procedure

At 0° C., N,N-dimethylformamide (2 mL, 27 mmol) was added to a solution of 3-methyl-thiazolidine-2,4-dione (33a) (1.77 g, 13.5 mmol) in phosphorus oxychloride (3.77 mL, 40.5 mmol). The reaction mixture was stirred at 110° C. for 3 hours, cooled to room temperature and quenched with a mixture of ice and ethyl acetate. The organic layer was washed with water (30 mL), brine (30 mL), dried over sodium sulfate, filtered, and evaporated under reduced pressure to give the desired aldehyde (33b) as a yellow solid (1.9 g, 10.7 mmol, 79%).

Workup

  1. temperaturecooled to room temperature
  2. customquenched with a mixture of ice and ethyl acetate
  3. washThe organic layer was washed with water (30 mL), brine (30 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-b6f1dd6fc2ea4f88b95b7a9d7441b29b
Source dataset
uspto-grants-2016_01
Patent number
US09238026B2

Reaction notes

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