Hydrochloric Acid → Methyl 3-fluoro-4-formylbenzoate

HRID 2233057ノート

反応式

HRID 2233057 の反応式
[H-].[Na+].[F:3][C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH:13]=[O:14])[C:7]([OH:9])=[O:8].[CH3:15]I.Cl>CN(C=O)C>[CH3:15][O:8][C:7](=[O:9])[C:6]1[CH:10]=[CH:11][C:12]([CH:13]=[O:14])=[C:4]([F:3])[CH:5]=1

参加物

6

実験手順

60% NaH (0.14 mol) is added portionwise to a solution of 3-fluoro-4-formyl benzoic acid (3, 0.12 mol) in dry DMF (330 mL). The mixture is stirred at room temperature for 30 min. Methyl iodide (0.14 mol) is added dropwise to the mixture. After stirring at room temperature for 5 h, the reaction mixture is poured into 1 N HCl (ca. 1000 mL) and extracted twice with EtOAc. The combined organic layers are washed with saturated aqueous NaHCO3, brine, dried over MgSO4, and evaporated in vacuo to give crude 3-fluoro-4-formyl benzoic acid methyl ester (4).

後処理

  1. stirringAfter stirring at room temperature for 5 h
  2. extractionextracted twice with EtOAc
  3. washThe combined organic layers are washed with saturated aqueous NaHCO3, brine
  4. dry with materialdried over MgSO4
  5. customevaporated in vacuo

出典と根拠

ORDレコード
ord-eb3b4645849e44f5a76852583bc8f0ba
出典データセット
uspto-grants-2010_05
特許番号
US07709470B2

反応ノート

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