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Stannous Chloride → 3-Chloro-4-ethylaniline

HRID 1068640
ノート
印刷プレビュー

反応式

HRID 1068640 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9].Cl[Sn]Cl>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9])[NH2:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24479Stannous ChlorideHCID 41134491-Chloro-2-ethyl-5-nitrobenzene

生成物 1

HCID 211899483-Chloro-4-ethylaniline収率 98%

実験手順

A solution of 8.9 g (48 mmol) of 31 and 54.6 g (241 mmol) of SnCl2, 2H2O in 100 mL of absolute alcohol was refluxed for 1 h. It was evaporated to remove most of the solvent and the residue was treated with 2N NaOH to pH =9. The mixture was filtered and the solid was washed with methanol (10 mL) and ethyl acetate (200 mL). The filtrate was separated and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic solution was dried (MgSO4) and evaporated to leave 7.31 g (98%) of liquid. 1H NMR (CDCl3), 1.178 (t, 3, J=7.5), 2.639 (q, 2, J=7.4), 6.532 (dd, 1, J=2.2, 8.1), 6.700 (d, 1, J=2.2), 6.996 (d, 1, J=8.2).

後処理

  1. customIt was evaporated
  2. customto remove most of the solvent
  3. additionthe residue was treated with 2N NaOH
  4. filtrationThe mixture was filtered
  5. washthe solid was washed with methanol (10 mL) and ethyl acetate (200 mL)
  6. customThe filtrate was separated
  7. extractionthe aqueous phase was extracted with ethyl acetate (2×50 mL)
  8. dry with materialThe combined organic solution was dried (MgSO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-b21171d189604a6a8f981f86eaa8f99d
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06251903B1

反応ノート

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