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

Acetic Acid → 5-Methanesulfonyl-1-methyl-3-(trifluoromethyl)pyrazole

HRID 1670369
ノート
印刷プレビュー

反応式

HRID 1670369 の反応式
[CH3:1][N:2]1[C:6]([S:7][CH3:8])=[CH:5][C:4]([C:9]([F:12])([F:11])[F:10])=[N:3]1.OO.[OH2:15].C(O)(=[O:18])C>O.O.[O-][W]([O-])(=O)=O.[Na+].[Na+]>[CH3:8][S:7]([C:6]1[N:2]([CH3:1])[N:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:5]=1)(=[O:18])=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 176Acetic AcidHCID 784Hydrogen PeroxideHCID 962WaterHCID 593563841-Methyl-5-methylthio-3-(trifluoromethyl)pyrazole

生成物 1

HCID 593563985-Methanesulfonyl-1-methyl-3-(trifluoromethyl)pyrazole

試薬・触媒・溶媒 1

HCID 150191Sodium Tungstate Dihydrate触媒

実験手順

0.25 g of Compounds (14) was dissolved in 20 ml of acetic acid. While stirring, 0.44 g of 30% hydrogen peroxide solution, and 0.04 g of sodium tungstate dihydrate were added sequentially. The mixture was stirred at room temperature for 12 hours, then poured into water, and extracted with ethyl acetate. The organic layer was washed with saturated sodium hydrogencarbonate, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure to produce 0.29 g of 5-methanesulfonyl-1-methyl-3-(trifluoromethyl)pyrazole (2-1).

後処理

  1. stirringThe mixture was stirred at room temperature for 12 hours
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with saturated sodium hydrogencarbonate
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-42b6c6a74d7c4e57b1b24da8832acf29
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07994094B2

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