Hydrochloric Acid → (2S)-3,3,3-trifluoro-2-hydroxypropanoic acid

HRID 1365540노트

반응식

HRID 1365540 반응식
[F:1][C:2]([F:10])([F:9])[C@@H:3]([OH:8])[C:4](C#N)=[O:5].[OH-:11].[Na+].OO.Cl>>[F:1][C:2]([F:10])([F:9])[C@@H:3]([OH:8])[C:4]([OH:11])=[O:5]

참가 물질

5

반응 조건

온도
65 °C

실험 절차

To a flask charged with (S)-3,3,3-trifluoro-2-hydroxypropanoyl cyanide (139 mg, 1 mmol) was added 3 N NaOH (6 mL) and 30% H2O2 (2.25 mL). The reaction mixture was heated at 65° C. for 1 h, then at 100° C. for a further 1 h. The reaction mixture was allowed to cooled to room temperature over 1 hr, then cool to 0° C. and the solution acidified with 6 N HCl (3 mL). The aqueous portion was extracted with ether (4×10 mL). The combined organic portions were dried over MgSO4, filtered and concentrated to give (S)-3,3,3-trifluoro-2-hydroxypropanoic acid as a clear oil (129 mg, 90% yield). NMR: 400 MHz 1H (CDCl3) 4.45 ppm, 1 H, m; 2.77 ppm, 2 H, m.

후처리

  1. temperatureto cooled to room temperature over 1 hr
  2. temperaturecool to 0° C.
  3. extractionThe aqueous portion was extracted with ether (4×10 mL)
  4. dry with materialThe combined organic portions were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7049e37e761a4a1d969ad5f78ba16b27
출처 데이터셋
uspto-grants-2011_02
특허 번호
US07888376B2

반응 노트

불러오는 중…