2-Bromo-4-nitroanisole → 2-Bromo-4-nitrophenol

HRID 458086

反応式

HRID 458086 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:11]C>CN(C=O)C.CCOC(C)=O.Cl>[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11]

参加物

5

反応条件

温度
115 °C

実験手順

2-Bromo4-nitroanisole (20 g, 0.086 mol) was dissolved in DMF (414 mL) at rt under N2. Sodium ethylthiolate (17.4 g, 0.207 mol) was added and the reaction mixture was warmed to 115° C. for 2 h. The reaction was cooled to rt and diluted with EtOAc (200 mL) and 1 M HCl (aq., 200 mL). The phases were separated, and the desired product was extracted into 1 M NaOH (aq, 150 mL×3). The basic aqueous extracts were combined and acidified using conc. HCl. The desired product was extracted from the acidic aqueous solution using EtOAc (250 mL×2). The combined organic layers were washed with brine and dried over sodium sulfate. The volatiles were removed in vacuo to afford a light brown semi-solid (9.8 g, 52% yield). 1H NMR (DMSO-d6) δ 8.33 (m, 1H); 8.09 (m, 1H); 7.07 (d, 1H).

後処理

  1. temperatureThe reaction was cooled to rt
  2. customThe phases were separated
  3. extractionthe desired product was extracted into 1 M NaOH (aq, 150 mL×3)
  4. extractionThe desired product was extracted from the acidic aqueous solution
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over sodium sulfate
  7. customThe volatiles were removed in vacuo

出典と根拠

ORDレコード
ord-8c964f0ad2554b1996530ab96f95cdac
出典データセット
uspto-grants-2007_03
特許番号
US07189734B2

関連ノート

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