Potassium Permanganate → (R)-2,2,2-trifluoro-N-(4-oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetamide

HRID 1363225노트

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HRID 1363225 반응식
[F:1][C:2]([F:17])([F:16])[C:3]([NH:5][C@H:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH2:8][CH2:7]1)=[O:4].[O-:18][Mn](=O)(=O)=O.[K+]>CC(C)=O.O>[F:1][C:2]([F:16])([F:17])[C:3]([NH:5][C@H:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9](=[O:18])[CH2:8][CH2:7]1)=[O:4]

참가 물질

5

실험 절차

To a solution of (R)-2,2,2-trifluoro-N-(1,2,3,4-tetrahydronaphthalen-1-yl)acetamide (1 g) in acetone (30 mL) at 0° C. was added a solution of MgSO4.7H2O (2.0 g) in water (15 mL). After 5 min of stirring, KMnO4 (2 g) was added in small portions over 1 hr. The mixture was then stirred overnight, slowly warming to room temp. Celite was added and the mixture was filtered. The filtrate was treated with saturated sodium metabisulfite and filtered. The filtrate was extracted with DCM several times. The combined organic extracts were washed with distilled water and brine, dried over MgSO4 and concentrated in vacuo to afford 0.96 g (91%) of the title compound, whose purity was good enough to use crude. 1H-NMR (300 MHz, CDCl3) □ 8.2 (d, 1H), 7.7 (t, 1H), 7.6 (t, 1H), 7.5 (d, 1H), 6.8 (broad s, 1H), 5.5 (m, 1H), 2.9 (m, 2H), 2.6 (m 1H), 2.4 (m, 1H) ppm.

후처리

  1. stirringThe mixture was then stirred overnight
  2. additionCelite was added
  3. filtrationthe mixture was filtered
  4. additionThe filtrate was treated with saturated sodium metabisulfite
  5. filtrationfiltered
  6. extractionThe filtrate was extracted with DCM several times
  7. washThe combined organic extracts were washed with distilled water and brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-1b165cc1054440ce898995f7fa79f698
출처 데이터셋
uspto-grants-2011_02
특허 번호
US07884109B2

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