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

Ethanesulfonyl chloride → N-(4-fluoro-3-nitrophenyl)ethanesulfonamide

HRID 36793
ノート
印刷プレビュー

反応式

HRID 36793 の反応式
[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[CH2:12]([S:14](Cl)(=[O:16])=[O:15])[CH3:13]>N1C=CC=CC=1>[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][S:14]([CH2:12][CH3:13])(=[O:16])=[O:15])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10]
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 11667Ethanesulfonyl chlorideHCID 677684-Fluoro-3-nitroaniline

生成物 1

HCID 3286362N-(4-fluoro-3-nitrophenyl)ethanesulfonamide収率 93%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

20.2 g (0.129 mol) of 4-fluoro-3-nitroaniline was dissolved in 120 ml of pyridine, and 17.8 g (0.136 mol) of ethanesulfonyl chloride was added dropwise to the solution at a temperature of not higher than 5° C. Thereafter the temperature was raised to room temperature and the reaction was continued for one night. After the pyridine was distilled off, the thus-obtained product was dissolved in ethyl acetate and washed with diluted hydrochloric acid twice, then with water, and with saturated saline solution. The solution was dried over anhydrous sodium sulfate, and the ethyl acetate was distilled off to obtain the crude product (crystals). The crude product was washed with diisopropyl ether, thereby obtaining 29.7 g of the objective product (yield: 93%) in the form of brown crystals. Melting point: 133° to 136° C.

後処理

  1. waitthe reaction was continued for one night
  2. distillationAfter the pyridine was distilled off
  3. dissolutionthe thus-obtained product was dissolved in ethyl acetate
  4. washwashed with diluted hydrochloric acid twice
  5. dry with materialThe solution was dried over anhydrous sodium sulfate
  6. distillationthe ethyl acetate was distilled off
  7. customto obtain the crude product (crystals)
  8. washThe crude product was washed with diisopropyl ether

出典と根拠

ORDレコード
ord-0de8c25ef53b4f38b1dc4201c18a173f
出典データセット
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05416236

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