Dimethylformamide → 57805-14-8
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
- temperaturecooled to room temperature
- customquenched with a mixture of ice and ethyl acetate
- washThe organic layer was washed with water (30 mL), brine (30 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- 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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