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Water → 2-Chloro-4-fluoro-6-nitroaniline

HRID 53698
ノート
印刷プレビュー

反応式

HRID 53698 の反応式
[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[Cl:12]N1C(=O)CCC1=O.O>CN(C=O)C>[Cl:12][C:7]1[CH:8]=[C:2]([F:1])[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[C:5]=1[NH2:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 31398ChlorosuccinimideHCID 677694-Fluoro-2-nitroaniline

生成物 1

HCID 199585612-Chloro-4-fluoro-6-nitroaniline

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

2-Chloro-4-fluoro-6-nitroaniline was prepared using an adaptation of the method of Mitchell, et al. (Mitchell, R. H. et al., J. Org. Chem. 44: 4733 (1979)). To a solution of 4-fluoro-2-nitroaniline (500 mg, 3.2 mmol) in dry DMF (10 mL) under N2 was added dropwise a solution of N-chlorosuccinimide (426 mg, 3.2 mmol) in dry DMF (16 mL). The reaction was allowed to stir overnight. The solution was then poured into 100 mL H2O and the resulting cloudy suspension extracted with 4×25 mL ethyl acetate. The combined organic phases were washed with 4×25 mL H2O and 25 mL saturated NaCl solution and dried (MgSO4). The MgSO4 was vacuum filtered and the solvent rotary evaporated to yield a brown crystalline solid which was purified further by flash chromatography (2:1 hexanes:ethyl acetate) to yield 424 mg of an orange crystalline solid (69.5%) 1H NMR (CDCl3) δ 6.46 (br s, 2H, NH2), 7.42 (dd, JH5-3 =3 Hz, JH3-F =7.2 Hz, H-4), 7.85 (dd, JH5-3 =3 Hz, JH5-F =8.7 Hz, H-5)

後処理

  1. extractionthe resulting cloudy suspension extracted with 4×25 mL ethyl acetate
  2. washThe combined organic phases were washed with 4×25 mL H2O and 25 mL saturated NaCl solution
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent rotary evaporated
  6. customto yield a brown crystalline solid which
  7. customwas purified further by flash chromatography (2:1 hexanes:ethyl acetate)

出典と根拠

ORDレコード
ord-4e3b15c66ebf45719cb89ad99ff610d7
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05620979

反応ノート

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