Trimethyl orthoformate → Methyl (E)-4-Chloro-3-methoxy-2-butenoate

HRID 868662

반응식

HRID 868662 반응식
[CH3:1][O:2][C:3](=[O:9])[CH2:4][C:5]([CH2:7][Cl:8])=[O:6].[CH3:10]OC(OC)OC>>[CH3:1][O:2][C:3](=[O:9])/[CH:4]=[C:5](/[O:6][CH3:10])\[CH2:7][Cl:8]

참가 물질

3

반응 조건

온도
150 °C

실험 절차

31.0 g (0.2 mol) of 4-chloro aceto acetic acid methyl ester was mixed with 106.0 g (1.0 mol) of orthoformic acid trimethyl ester. 30.0 g of Amberlyst-15 ion exchange resin was added under argon with stirring. The reaction temperature rose to 40° C. with vigorous development of gas. After 5 hours of stirring, no educt could any longer be detected by thin-layer chromatography. The ion exchange resin was filtered off, and the residue was distilled in a water jet vacuum. The distillate was mixed with 1.0 g of p-toluenesulfonic acid monohydrate and slowly heated to 150° C., whereby methanol distilled off. The reaction mass was then distilled in a water jet vacuum. 24.7 g of a colorless liquid with a boiling point bp12 =93° C. was obtained.

후처리

  1. addition30.0 g of Amberlyst-15 ion exchange resin was added under argon
  2. customrose to 40° C. with vigorous development of gas
  3. stirringAfter 5 hours of stirring
  4. filtrationThe ion exchange resin was filtered off
  5. distillationthe residue was distilled in a water jet vacuum
  6. additionThe distillate was mixed with 1.0 g of p-toluenesulfonic acid monohydrate
  7. distillationwhereby methanol distilled off
  8. distillationThe reaction mass was then distilled in a water jet vacuum

출처 및 근거

ORD 기록
ord-bbb113d490c44f34bd0fc9d8e9eda19b
출처 데이터셋
uspto-grants-1988_10
특허 번호
US04780545

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