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Ethyl formate → Ethyl 2-formyl-3-oxopropanoate

HRID 12854
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HRID 12854 반응식
C(O[CH:4]([O:11]CC)[CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])C.[CH:14](OCC)=[O:15].C(O[K])(C)(C)C>C1COCC1>[CH2:9]([O:8][C:6](=[O:7])[CH:5]([CH:4]=[O:11])[CH:14]=[O:15])[CH3:10]
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참가 물질

5

반응물 3

HCID 8025Ethyl formateHCID 66389Ethyl 3,3-diethoxypropionateHCID 178418922HCID 178418922, 화합물

생성물 1

HCID 11029955Ethyl 2-formyl-3-oxopropanoate수율 100.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

Ethyl 3,3-diethoxypropionate (100 g, 525.7 mmol) was dissolved in THF (360 ml) at room temp. Ethyl formate (175.1 ml, 2.1 mol) was added at room temp. The solution was cooled in an ice-bath to 0° C. and tBuOK (1M solution in THF, 1,156 ml, 1.156 mol) was added via an addition funnel slowly over 30 min, maintaining internal temperature below 5° C. The color changed instantly from colorless to dark orange. The reaction mixture was allowed to warm up to room temp. and stirred for 2 h. The reaction was allowed to stir at room temp. for 18 h. The reaction mixture was concentrated in vacuo and 1 L of solvent was removed. The remaining brownish solution with white solid in it was cooled in an ice-bath and hydrochloric acid (6N, 200 ml) was added to adjust pH=3, maintaining internal temperature below 20° C. The resulting bright yellow suspension was then warmed up to room temp. and stirred for 1 h. Additional 700 ml solvent was removed in vacuo at room temp. Water (400 ml) was added to dissolve all the white solid and ethyl acetate (500 ml) was added and the mixture transferred to a separatory funnel. The aqueous was extracted once with ethyl acetate (200 ml). The combined organic extracts was washed once with brine (100 ml). After drying over MgSO4 and concentrating in vacuo, 2-formyl-3-oxo-propionic acid ethyl ester (75.85 g) was obtained as yellow oil.

후처리

  1. temperaturemaintaining internal temperature below 5° C
  2. temperatureto warm up to room temp.
  3. stirringto stir at room temp. for 18 h
  4. concentrationThe reaction mixture was concentrated in vacuo and 1 L of solvent
  5. customwas removed
  6. temperatureThe remaining brownish solution with white solid in it was cooled in an ice-bath
  7. additionhydrochloric acid (6N, 200 ml) was added
  8. temperaturemaintaining internal temperature below 20° C
  9. temperatureThe resulting bright yellow suspension was then warmed up to room temp.
  10. stirringstirred for 1 h
  11. customAdditional 700 ml solvent was removed in vacuo at room temp
  12. additionWater (400 ml) was added
  13. dissolutionto dissolve all the white solid and ethyl acetate (500 ml)
  14. additionwas added
  15. customthe mixture transferred to a separatory funnel
  16. extractionThe aqueous was extracted once with ethyl acetate (200 ml)
  17. washThe combined organic extracts was washed once with brine (100 ml)
  18. dry with materialAfter drying over MgSO4
  19. concentrationconcentrating in vacuo

출처 및 근거

ORD 기록
ord-f162d2aee57f4371ba5eb6e5a8135f3d
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728029B2

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