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

Ammonia → 4-Cyclopropyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

HRID 745727
ノート
印刷プレビュー

反応式

HRID 745727 の反応式
[CH:1]1([C:4]2[N:9]=[C:8]([C:10]([Cl:13])([Cl:12])[Cl:11])[N:7]=[C:6](C(Cl)(Cl)Cl)[N:5]=2)[CH2:3][CH2:2]1.[NH3:18]>O1CCCC1.O>[NH2:18][C:6]1[N:5]=[C:4]([CH:1]2[CH2:2][CH2:3]2)[N:9]=[C:8]([C:10]([Cl:13])([Cl:12])[Cl:11])[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 222AmmoniaHCID 201996132-Cyclopropyl-4,6-bis-trichloromethyl-1,3,5-triazine

生成物 1

HCID 201996154-Cyclopropyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

71.2 g of 2-cyclopropyl-4,6-bis-trichloromethyl-1,3,5-triazine are dissolved in 70 ml of tetrahydrofuran, and at room temperature are added, with stirring, 300 ml of a concentrated aqueous ammonia solution. The reaction mixture is stirred for 30 minutes; it is then diluted with water, and the formed emulsion is extracted with ether. The ether phases are collected, dried, filtered and subsequently concentrated by evaporation. The residue crystallises and there remain 48 g of the crystalline title product, m.p. 111°-114° C.

後処理

  1. additionat room temperature are added
  2. stirringThe reaction mixture is stirred for 30 minutes
  3. extractionthe formed emulsion is extracted with ether
  4. customThe ether phases are collected
  5. customdried
  6. filtrationfiltered
  7. concentrationsubsequently concentrated by evaporation
  8. customThe residue crystallises

出典と根拠

ORDレコード
ord-987410bd30604bcf9e2439a22ae8bbb6
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04600428

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