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

Hydrochloric Acid → 4-Amino-5,6-dichloropicolinic Acid

HRID 2407809
ノート
印刷プレビュー

反応式

HRID 2407809 の反応式
[NH2:1][C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([O:12]C)=[O:11])[CH:3]=1.C[Si](C)(C)[O-].[K+].Cl.C(OCC)(=O)C>O1CCCC1.O>[NH2:1][C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([OH:12])=[O:11])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 23668039Potassium trimethylsilanolateHCID 58504072Methyl 4-amino-5,6-dichloro-2-pyridinecarboxylate

生成物 1

HCID 585040704-Amino-5,6-dichloropicolinic Acid収率 98.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒

実験手順

The compound prepared in Example 405 (2.438 g) and potassium trimethylsilanolate (2.971 g) were suspended in tetrahydrofuran (100 mL) and stirred at reflux for 4 hours. The reaction mixture was dissolved in water and added to 1 N hydrochloric acid. Ethyl acetate was added and the system stirred at room temperature. The organics were dried, magnesium sulfate and concentrated under reduced pressure to furnish the title compound (2.250 g), which was used without further purification, possessing the following physical data.

後処理

  1. temperatureat reflux for 4 hours
  2. stirringthe system stirred at room temperature
  3. customThe organics were dried
  4. concentrationmagnesium sulfate and concentrated under reduced pressure

出典と根拠

ORDレコード
ord-2d3e1c67be8e44c29e6804966f15762b
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08809538B2

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
HCID 8028
Tetrahydrofuran
溶媒