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

Water → HCID 15579464、化合物

HRID 1721832
ノート
印刷プレビュー

反応式

HRID 1721832 の反応式
[C:1]([C:4]1[CH:5]=[CH:6][C:7]([CH3:14])=[C:8]([S:10]([NH2:13])(=[O:12])=[O:11])[CH:9]=1)(=[O:3])[CH3:2].[Br:15]Br.O>CO>[Br:15][CH2:2][C:1]([C:4]1[CH:5]=[CH:6][C:7]([CH3:14])=[C:8]([S:10]([NH2:13])(=[O:11])=[O:12])[CH:9]=1)=[O:3]
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 3

HCID 962WaterHCID 24408BromineHCID 126197975-Acetyl-2-methylbenzene-1-sulfonamide

生成物 1

HCID 15579464HCID 15579464、化合物収率 95.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

21.3 Grams (0.1 M) of 5-acetyl-2-methylbenzenesulfonamide was dissolved in 180 g of methanol, while the resulting solution was kept at 35°-40° C., 16.0 g (0.1 M) of bromine was added dropwise by taking 1.5 hours. The reaction mixture was stirred for 10 minutes after the dropwise addition, 80 g of water was added to the reaction mixture and the whole reaction mixture was stirred for further 30 minutes at room temperature. A part of methanolwater was removed by evaporation, then the crystals formed were collected by filtration, washed with water and dried to obtain 28.0 g of 5-bromoacetyl-2-methylbenzenesulfonamide in the form of white crystals. Melting point: 146.5°-147.5° C Yield: 95.9%.

後処理

  1. customwas kept at 35°-40° C.
  2. additionwas added to the reaction mixture
  3. customthe whole reaction mixture
  4. stirringwas stirred for further 30 minutes at room temperature
  5. customA part of methanolwater was removed by evaporation
  6. customthe crystals formed
  7. filtrationwere collected by filtration
  8. washwashed with water
  9. customdried

出典と根拠

ORDレコード
ord-ca5f3c63e82349399f3fc79049391fe8
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04853158

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