4-Methoxy-2-nitrobenzonitrile → 4-Hydroxy-2-nitrobenzonitrile

HRID 711727

反応式

HRID 711727 の反応式
C[O:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1.Cl.N1C=CC=CC=1>>[OH:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[C:5]([N+:11]([O-:13])=[O:12])[CH:4]=1

参加物

3

反応物 2

HCID 2886654-Methoxy-2-nitrobenzonitrileHCID 10176127Pyridinium chloride

生成物 1

HCID 534181214-Hydroxy-2-nitrobenzonitrile収率 26.5%

反応条件

温度
200 °C

実験手順

A mixture of 4-methoxy-2-nitrobenzonitrile (820 mg, 4.6 mmol) and pyridine hydrochloride (755 mg, 4.6 mmol) was heated at 200° C. under N2 for 18 hours. Upon completion, the reaction was cooled to room temperature, washed with brine and extracted with EtOAc (2×100 mL). The organic layers were combined, dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (1:1 Hexane:EtOAc) to provide 4-hydroxy-2-nitrobenzonitrile (200 mg, 26%). 1H NMR (400 MHz, MeOD) δ 7.24 (dd, J=8.6, 2.4 Hz, 1H), 7.70 (d, J=2.4 Hz, 1H), 7.83 (d, J=8.6 Hz, 1H).

後処理

  1. temperatureUpon completion, the reaction was cooled to room temperature
  2. washwashed with brine
  3. extractionextracted with EtOAc (2×100 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by flash chromatography (1:1 Hexane:EtOAc)

出典と根拠

ORDレコード
ord-0d10c11930fd425b9418cb88afde6fe6
出典データセット
uspto-grants-2015_11
特許番号
US09181276B2

関連ノート

読み込み中…