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

HRID 965916ノート

反応式

HRID 965916 の反応式
[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

参加物

6

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-f2ede5a651fd45438204057c0060ff10
出典データセット
uspto-grants-2005_10
特許番号
US06951874B2

反応ノート

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