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

Dichloromethane → Methyl 2,6-dichloro-4-nitrobenzoate

HRID 1060484
ノート
印刷プレビュー

反応式

HRID 1060484 の反応式
[Cl:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([Cl:14])[C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH2:19](Cl)Cl>>[Cl:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([Cl:14])[C:3]=1[C:4]([O:6][CH3:19])=[O:5]
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 3

HCID 6344DichloromethaneHCID 24386Thionyl ChlorideHCID 225719382,6-Dichloro-4-nitrobenzoic acid

生成物 1

HCID 22571909Methyl 2,6-dichloro-4-nitrobenzoate収率 80%

実験手順

To 2,6-dichloro-4-nitrobenzoic acid (12.8 g, U.S. Pat. No. 3,423,475) was added anhydrous CH2Cl2 (60 mL) and thionyl chloride (40 mL) then the resulting mixture was refluxed for 19 h. The mixture was allowed to cool to room temperature and evaporated. Additional CH2Cl2 (10 mL) was added and the solution was evaporated. MeOH (100 mL) was added to the residue and the mixture was refluxed for 17 h. The mixture was allowed to cool to room temperature and placed in an ice-bath. The precipitated solid was collected by filtration to give methyl 2,6-dichloro-4-nitrobenzoate (10.8 g, 80%).

後処理

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
  1. temperaturethe resulting mixture was refluxed for 19 h
  2. customevaporated
  3. additionAdditional CH2Cl2 (10 mL) was added
  4. customthe solution was evaporated
  5. additionMeOH (100 mL) was added to the residue
  6. temperaturethe mixture was refluxed for 17 h
  7. temperatureto cool to room temperature
  8. customplaced in an ice-bath
  9. filtrationThe precipitated solid was collected by filtration

出典と根拠

ORDレコード
ord-50b3fa2aa25947b9b1a6e77e8ef78100
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06521666B1

反応ノート

読み込み中…