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

Sulfuric Acid → 2-Chloro-5-Fluorobenzaldehyde

HRID 49195
ノート
印刷プレビュー

反応式

HRID 49195 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH3:9].S(=O)(=O)(O)[OH:11]>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1118Sulfuric AcidHCID 1184752-Chloro-5-fluorotoluene

生成物 1

HCID 27791842-Chloro-5-Fluorobenzaldehyde

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒2 回

実験手順

A solution of 2-chloro-5-fluorotoluene (5.0 g) in acetic anhydride (40 ml) was treated dropwise with concentrated sulfuric acid (40 ml) with cooling on ice. Subsequently, a solution of chromic anhydride (9.3 g) in acetic anhydride (40 ml) was added dropwise over a period of 2 hours. At the same temperature, the mixture was stirred for 1 hour, and added to an ice-water. The mixture was extracted with diethyl ether and the organic layer was washed successively with aqueous sodium carbonate, water and saturated brine, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was dissolved in tetrahydrofuran (10 ml), combined with water (4 ml) and concentrated sulfuric acid (4 ml), and heated with stirring at 100° C. for 30 minutes. After allowed to stand to cool, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed successively with aqueous sodium carbonate, water and saturated brine, and dried over magnesium sulfate. The solvent was distilled off and the residue was subjected to a column chromatography on a silica gel to obtain 2-chloro-5-fluorobenzaldehyde (1.6 g).

後処理

  1. temperaturewith cooling on ice
  2. extractionThe mixture was extracted with diethyl ether
  3. washthe organic layer was washed successively with aqueous sodium carbonate, water and saturated brine
  4. dry with materialdried over magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. dissolutionthe residue was dissolved in tetrahydrofuran (10 ml)
  7. temperatureheated
  8. stirringwith stirring at 100° C. for 30 minutes
  9. temperatureto cool
  10. extractionthe reaction mixture was extracted with ethyl acetate
  11. washthe organic layer was washed successively with aqueous sodium carbonate, water and saturated brine
  12. dry with materialdried over magnesium sulfate
  13. distillationThe solvent was distilled off

出典と根拠

ORDレコード
ord-68a37d73731c4dc9b70bfce304b4484d
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06706732B1

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