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

4-Methoxybenzenesulfonyl chloride → HCID 247207、化合物

HRID 1879442
ノート
印刷プレビュー

反応式

HRID 1879442 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9](Cl)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[NH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)(=[O:11])=[O:10])=[CH:5][CH:4]=1
参加物反応条件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 74014-Methoxybenzenesulfonyl chlorideHCID 31268Pyrrolidine

生成物 1

HCID 247207HCID 247207、化合物収率 91.6%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

反応条件

温度
0 °C

実験手順

4-Methoxy-benzenesulfonyl chloride (3.00 g, 14.52 mmol) was slowly added to a solution of pyrrolidine (5.15 g, 72.6 mmol) in CHCl3 (15 mL) with stirring at 0° C. The reaction mixture was allowed to warm up to room temperature and then stirred for 1 hour. After that the reaction mixture was concentrated in vacuo. The residue was dissolved in toluene and washed with aqueous H3PO4 solution, and then aqueous KHCO3 solution. The organic phase was dried with Na2SO4, and filtered. The solvents were removed in vacuo and the residue crystallized from ether and heptane to provide the title compound (3.21 g, m.p. 88-89° C.).

後処理

  1. temperatureto warm up to room temperature
  2. stirringstirred for 1 hour
  3. concentrationAfter that the reaction mixture was concentrated in vacuo
  4. dissolutionThe residue was dissolved in toluene
  5. washwashed with aqueous H3PO4 solution
  6. dry with materialThe organic phase was dried with Na2SO4
  7. filtrationfiltered
  8. customThe solvents were removed in vacuo
  9. customthe residue crystallized from ether and heptane

出典と根拠

ORDレコード
ord-aaca5289b4d24e1ca92015dce9d49172
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08314270B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート