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Nitric Acid → 5-Chloro-4-nitrothiophene-2-carbaldehyde

HRID 1192060
ノート
印刷プレビュー

反応式

HRID 1192060 の反応式
[Cl:1][C:2]1[S:6][C:5]([CH:7]=[O:8])=[CH:4][CH:3]=1.[N+:9]([O-])([OH:11])=[O:10]>>[Cl:1][C:2]1[S:6][C:5]([CH:7]=[O:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10]
参加物反応条件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 944Nitric AcidHCID 817002-Thiophenecarboxaldehyde, 5-chloro-

生成物 1

HCID 602073145-Chloro-4-nitrothiophene-2-carbaldehyde収率 58%

反応条件

温度
-5 °C

実験手順

5-Chlorothiophene-2-carbaldehyde (2.0 g, 13.6 mmol) was added dropwise to a stirred fuming nitric acid (13 mL) cooled to −5° C. with an ice/methanol bath. When addition was complete the stirred reaction mixture was allowed to warm slowly to 5° C. over 1 hour, then it was poured into ice/water (200 mL). The precipitated solid was collected by filtration, dissolved in dichloromethane (100 mL), washed with water and the organic layer was separated and dried (MgSO4). After filtration the solvent was removed under reduced pressure and the residual brown solid was crystallised from hexane (insoluble brown material was removed by decantation of the supernatant solution), to afford title product as an off-white solid (1.51 g, 58%). 1H NMR (300 MHz, CDCl3) δ: 9.83 (1H, s), 8.20 (1H, s).

後処理

  1. additionWhen addition
  2. customthe stirred reaction mixture
  3. temperatureto warm slowly to 5° C. over 1 hour
  4. filtrationThe precipitated solid was collected by filtration
  5. dissolutiondissolved in dichloromethane (100 mL)
  6. washwashed with water
  7. customthe organic layer was separated
  8. dry with materialdried (MgSO4)
  9. filtrationAfter filtration the solvent
  10. customwas removed under reduced pressure
  11. customthe residual brown solid was crystallised from hexane (insoluble brown material
  12. customwas removed by decantation of the supernatant solution),

出典と根拠

ORDレコード
ord-0131aee8af204fabba77e0369bd5f634
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08680139B2

反応ノート

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