Methyl chloroformate → (2S,3S)-3-methoxy-2-(methoxycarbonylamino)butanoic acid

HRID 1471050노트

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HRID 1471050 반응식
[CH3:1][O:2][C@H:3]([CH3:9])[C@@H:4]([C:6]([OH:8])=[O:7])[NH2:5].Cl[C:11]([O:13][CH3:14])=[O:12]>C(=O)(O)[O-].[Na+]>[CH3:1][O:2][C@@H:3]([CH3:9])[C@H:4]([NH:5][C:11]([O:13][CH3:14])=[O:12])[C:6]([OH:8])=[O:7]

참가 물질

4

실험 절차

A solution of allo-O-methyl-L-threonine (519 mg, 3.90 mmol) in saturated sodium bicarbonate solution (47.6 mL) was treated dropwise with methyl chloroformate (453 μL, 553 mg, 5.85 mmol) followed by stirring at RT for 18 h. The mixture was extracted with ether and the aqueous phase was cooled to 0° C. and acidified to pH 2-3 by addition of concentrated hydrochloric acid solution. The mixture was extracted with ethyl acetate (3×). The combined organic layers were extracted with saturated sodium chloride solution and dried (Na2SO4). Concentration in vacuo afforded the title compound (640 mg, 86%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 5.48 (d, J=7.8 Hz, 1H), 4.52 (d, J=4.7 Hz, 1H), 3.71 (s, 3H), 3.39 (s, 3H), 1.25 (t, J=7.6 Hz, 3H).

후처리

  1. extractionThe mixture was extracted with ether
  2. temperaturethe aqueous phase was cooled to 0° C.
  3. additionacidified to pH 2-3 by addition of concentrated hydrochloric acid solution
  4. extractionThe mixture was extracted with ethyl acetate (3×)
  5. extractionThe combined organic layers were extracted with saturated sodium chloride solution
  6. dry with materialdried (Na2SO4)
  7. concentrationConcentration in vacuo

출처 및 근거

ORD 기록
ord-5d2f9ff49bfe4c2e8b8ceb47afbe662a
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09006387B2

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