Methyl α-hydroxy-2,4-dinitro-α-(trifluoromethyl)benzeneacetate → HCID 59395032、化合物

HRID 1958544ノート

反応式

HRID 1958544 の反応式
[N+:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:5]=1[C:13]([OH:22])([C:18]([F:21])([F:20])[F:19])[C:14](OC)=[O:15])([O-])=O>C(OCC)(=O)C>[NH2:10][C:8]1[CH:9]=[C:4]2[C:5]([C:13]([OH:22])([C:18]([F:21])([F:20])[F:19])[C:14](=[O:15])[NH:1]2)=[CH:6][CH:7]=1

参加物

3

実験手順

To a solution of methyl 2-(2,4-dinitrophenyl)-3,3,3-trifluoro-2-hydroxypropanoate (1.3 g, 4.01 mmol) in ethyl acetate (18 mL) was successively added pH3HCl (5.2 mL), then PdC (350 mg) in ethyl acetate (3 mL). The mixture was vigorously stirred overnight under H2 (1 atm). The catalyst was filtered off through Celite and the filtrate was concentrated to dryness. The crude residue obtained was partitioned between DCM (25 mL) and aqueous saturated NaHCO3 (15 mL). The organic phase was separated and the aqueous phase was extracted DCM (2×25 mL). The organic phases were combined, dried over sodium sulfate, filtered, and concentrated. The crude residue obtained was purified by silica gel column chromatography using a gradient 50-100% ethyl acetate in hexanes to give 6-amino-3-hydroxy-3-(trifluoromethyl)indolin-2-one (921 mg, 99%)

後処理

  1. filtrationThe catalyst was filtered off through Celite
  2. concentrationthe filtrate was concentrated to dryness
  3. customThe crude residue obtained
  4. customwas partitioned between DCM (25 mL) and aqueous saturated NaHCO3 (15 mL)
  5. customThe organic phase was separated
  6. extractionthe aqueous phase was extracted DCM (2×25 mL)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude residue obtained
  11. customwas purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-b8fbfd83797f427dbe195b9f139b0bc7
出典データセット
uspto-grants-2013_04
特許番号
US08410132B2

反応ノート

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