Dimethylformamide → 4-Chloro-3-methyl-2-oxo-2,3-dihydro-1,3-thiazole-5-carbaldehyde

HRID 591058ノート

反応式

HRID 591058 の反応式
[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]

参加物

4

反応条件

温度
110 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-b6f1dd6fc2ea4f88b95b7a9d7441b29b
出典データセット
uspto-grants-2016_01
特許番号
US09238026B2

反応ノート

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