Ammonia → propan-2-yl (2S)-2-amino-3-methylbutanoate

HRID 2418940노트

반응식

HRID 2418940 반응식
C(=O)=O.CO.S(Cl)(Cl)=O.[NH2:10][C@H:11]([C:15]([OH:17])=[O:16])[CH:12]([CH3:14])[CH3:13].N.[CH:19]1[CH:20]=CC2C(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)OC(=O)C=2[CH:24]=1>O.CCOCC.C(O)(C)C>[CH:19]([O:16][C:15](=[O:17])[C@H:11]([CH:12]([CH3:14])[CH3:13])[NH2:10])([CH3:20])[CH3:24]

참가 물질

9

실험 절차

One hundred and twenty-five ml (1.64 mole) of isopropanol was cooled to -10° C with a freezing mixture of dry ice-methanol, and 30 ml (0.42 mole) of thionyl chloride was added dropwise thereto while stirring. Thereafter, 25 g (0.21 mole) of l-valine was added little by little while maintaining this temperature. The reaction mixture was first raised to room temperature gradually and then finally it was reacted at 100° C for 40 hours while stirring. After completion of the reaction, unreacted thionyl chloride and isopropanol were evaporated in vacuo. The residue obtained was dissolved in 10 to 20 ml of water. The solution was covered with 400 ml of ether and an aqueous ammonia was added thereto until the phenolphthalein indicator turned red. After extracting the solution with ether three to four times, the ether extract was dried over anhydrous sodium sulfate and distilled under reduced pressure to obtain a colorless and clear l-valine isopropyl ester (B.P. 40° - 41° C/3 - 4 mmHg).

후처리

  1. additionwas added dropwise
  2. temperaturewhile maintaining this temperature
  3. customfinally it was reacted at 100° C for 40 hours
  4. stirringwhile stirring
  5. customwere evaporated in vacuo
  6. customThe residue obtained
  7. extractionAfter extracting the solution with ether three to four times
  8. extractionthe ether extract
  9. dry with materialwas dried over anhydrous sodium sulfate
  10. distillationdistilled under reduced pressure

출처 및 근거

ORD 기록
ord-ce837109061042218638fd498bf8de54
출처 데이터셋
uspto-grants-1978_08
특허 번호
US04104040

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