ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Stannous chloride dihydrate → 3-Chloro-4-ethylaniline

HRID 1857431
ノート
印刷プレビュー

反応式

HRID 1857431 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].O.O.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 61436Stannous chloride dihydrateHCID 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 to pH=9
  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-1b898e2fbfe345118ecef498e6157780
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06147075

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート