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

1,1'-Thiocarbonyldiimidazole → HCID 22139828、化合物

HRID 2250506
ノート
印刷プレビュー

反応式

HRID 2250506 の反応式
[C:1]([N:8]1[CH:12]=[CH:11]N=C1)(N1C=CN=C1)=[S:2].NC1[C:18]([Cl:19])=[CH:17][S:16]C=1>C1COCC1>[Cl:19][C:18]1[C:12]([N:8]=[C:1]=[S:2])=[CH:11][S:16][CH:17]=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 2

HCID 802641,1'-ThiocarbonyldiimidazoleHCID 221398234-Chlorothiophen-3-amine

生成物 1

HCID 22139828HCID 22139828、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

1.46 g of thiocarbonyldiimidazole are added to a solution of 1.1 g of 3-amino-4-chlorothiophene in 20 ml of anhydrous THF, and the mixture is stirred at room temperature for one hour. The solid is distilled off under reduced pressure, the residue is dissolved in ethyl acetate, the organic phase is treated twice with water in a separating funnel and then dried, and the solvent is again distilled off under reduced pressure. This gives 4-chloro-3-thienyl isothiocyanate as a dark oil which is then reacted further without further purification steps.

後処理

  1. distillationThe solid is distilled off under reduced pressure
  2. dissolutionthe residue is dissolved in ethyl acetate
  3. additionthe organic phase is treated twice with water in a separating funnel
  4. customdried
  5. distillationthe solvent is again distilled off under reduced pressure
  6. customThis gives 4-chloro-3-thienyl isothiocyanate as a dark oil which is then reacted further without further purification steps

出典と根拠

ORDレコード
ord-f36ebc2000d845b58dfcb3f7f2894d27
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07317033B2

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