5-Fluoro-2-nitrophenol → (2S)-2-[(5-Fluoro-2-nitrophenoxy)methyl]oxirane

HRID 584634

반응식

HRID 584634 반응식
[CH2:1]1[O:3][C@@H:2]1[CH2:4][OH:5].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:25][C:26]1[CH:27]=[CH:28][C:29]([N+:33]([O-:35])=[O:34])=[C:30](O)[CH:31]=1.CCOC(/N=N/C(OCC)=O)=O>C1COCC1>[F:25][C:26]1[CH:31]=[CH:30][C:29]([N+:33]([O-:35])=[O:34])=[C:28]([CH:27]=1)[O:5][CH2:4][C@@H:2]1[CH2:1][O:3]1

참가 물질

6

실험 절차

In a flask was added (R)-glycidol (0.994 g, 13.4 mmole) and triphenylphosphine (3.52 g, 13.4 mmole) and THF (20 ml, dried over molecular sieves), and 5-fluoro-2-nitrophenol (2.10 g, 13.4 mmole). The mixture was stirred until a homogeneous solution was obtained. The solution was cooled in an ice bath and diethylazodicarboxylate (DEAD, 2.11 ml, 13.4 mmole) was added dropwise over a few minutes. After completed addition, the flask was allowed to reach room temperature and stirred for an additional 2 hours. The solvent was removed in vaccuo and to the residue was added chloroform (5-10 ml). The precipitate (PPh3O) was removed by filtration and the solid was washed with an additional amount of chloroform (5-10 ml). The filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1), and purified to give 2.02 g (71%) of the sub-title compound as a crystalline material after concentration of pure fractions.

후처리

  1. customwas obtained
  2. temperatureThe solution was cooled in an ice bath
  3. additionaddition
  4. customto reach room temperature
  5. stirringstirred for an additional 2 hours
  6. customThe solvent was removed in vaccuo and to the residue
  7. additionwas added chloroform (5-10 ml)
  8. customThe precipitate (PPh3O) was removed by filtration
  9. washthe solid was washed with an additional amount of chloroform (5-10 ml)
  10. additionThe filtrate was added to a flash column (SiO2, Heptane:Ethyl acetate 4:1)
  11. custompurified

출처 및 근거

ORD 기록
ord-a278d7879ffc4c68929b95b57a96a4f3
출처 데이터셋
uspto-grants-2005_08
특허 번호
US06927222B2

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