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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
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Ethanol → 2-Amino-4-ethoxy-6-trifluoromethoxy-1,3,5-triazine

HRID 249410
ノート
印刷プレビュー

反応式

HRID 249410 の反応式
[H-].[Na+].[NH2:3][C:4]1[N:9]=[C:8](F)[N:7]=[C:6]([O:11][C:12]([F:15])([F:14])[F:13])[N:5]=1.[CH2:16]([OH:18])[CH3:17]>>[NH2:3][C:4]1[N:9]=[C:8]([O:18][CH2:16][CH3:17])[N:7]=[C:6]([O:11][C:12]([F:15])([F:14])[F:13])[N:5]=1
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 702EthanolHCID 24758Sodium hydrideHCID 150103882-Amino-4-fluoro-6-trifluoromethoxy-1,3,5-triazin

生成物 1

HCID 150103952-Amino-4-ethoxy-6-trifluoromethoxy-1,3,5-triazine

実験手順

2.3 g (0.093 mol) of 97% sodium hydride were added a little at a time to 300 ml of ethanol at 20°-35° C. and dissolved by stirring for 15 minutes. Then, while stirring at 0° C., 18.5 g (0.093 mol) of 2-amino-4-fluoro-6-trifluoromethoxy-1,3,5-triazine were added over the course of 10 minutes, and the mixture was stirred at 0° C. for 1 hour and at 22° C. overnight. The residue from concentration under reduced pressure was taken up in methylene chloride, extracted with water and dried. Concentration yielded 17.9 g (85.9% of theory) of the title compound of melting point 69°-71° C.

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
  • dissolutiondissolved
  • stirringThen, while stirring at 0° C.
  • stirringthe mixture was stirred at 0° C. for 1 hour and at 22° C. overnight
  • concentrationThe residue from concentration under reduced pressure
  • extractionextracted with water
  • customdried
  • concentrationConcentration
  • 出典と根拠

    ORDレコード
    ord-da1c5f301465450ca9fdb924ddd48108
    出典データセット
    uspto-grants-1993_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05214143

    反応ノート

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