Dimethylformamide → 3-(Dimethoxymethyl)thiophene-2-carbaldehyde

HRID 26995ノート

反応式

HRID 26995 の反応式
[CH3:1][O:2][CH:3]([O:9][CH3:10])[C:4]1[CH:8]=[CH:7][S:6][CH:5]=1.C([Li])CCC.CN(C)[CH:18]=[O:19]>CCOCC>[CH3:1][O:2][CH:3]([O:9][CH3:10])[C:4]1[CH:8]=[CH:7][S:6][C:5]=1[CH:18]=[O:19]

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 159181383-(Dimethoxymethyl)thiopheneHCID 178418339Butyllithium

生成物 1

HCID 159181393-(Dimethoxymethyl)thiophene-2-carbaldehyde

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒3 回

実験手順

To a stirred solution of 2a (423 g., 2.68 moles) in anhydrous ether (1 L) was added dropwise in 1 hour a freshly prepared solution of n-butyllithium (27 moles) in ether keeping a gentle reflux under dry N2. Reflux being continued for 0.5 hour, a solution of DMF (dimethylformamide) (432 g., 6 moles) in anhydrous ether (0.8 L) was added dropwise to the mixture over a period of 0.75 hour with vigorous stirring. After the complete addition the mixture was stirred overnight, poured onto crushed ice (1 Kg.) with stirring and allowed to rise to room temperature. The organic layer was separated and the water layer was saturated with NaCl and extracted thoroughly with ether (2×200 ml.). The ether extracts were combined, dried over MgSO4 and concentrated. The residue was distilled under reduced pressure and the pale yellow oil was collected at 100°-125° C., 0.7 mmHg. Yield, 277 g. (56%).

後処理

  1. temperaturea gentle reflux under dry N2
  2. temperatureReflux
  3. additionAfter the complete addition the mixture
  4. additionpoured
  5. stirringwith stirring
  6. customto rise to room temperature
  7. customThe organic layer was separated
  8. extractionextracted thoroughly with ether (2×200 ml.)
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated
  11. distillationThe residue was distilled under reduced pressure
  12. customthe pale yellow oil was collected at 100°-125° C.
  13. customYield

出典と根拠

ORDレコード
ord-9a4f2f45d23f4ce1a0f87c9f0af97c04
出典データセット
uspto-grants-1979_04
特許番号
US04151352

反応ノート

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