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

HRID 26995노트

반응식

HRID 26995 반응식
[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]

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 159181383-(Dimethoxymethyl)thiopheneHCID 178418339Butyllithium

생성물 1

HCID 159181393-(Dimethoxymethyl)thiophene-2-carbaldehyde

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-9a4f2f45d23f4ce1a0f87c9f0af97c04
출처 데이터셋
uspto-grants-1979_04
특허 번호
US04151352

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