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 178524945、化合物

HRID 2064674
ノート
印刷プレビュー

反応式

HRID 2064674 の反応式
[CH3:1][C:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:5][NH:4][N:3]=1.[Mn]([O-])(=O)(=O)=[O:14].[K+].[OH2:19]>C(O)(C)(C)C>[C:7]1([C:6]2[C:2]([C:1]([OH:14])=[O:19])=[N:3][NH:4][CH:5]=2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
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 516875Potassium PermanganateHCID 178434528HCID 178434528、化合物

生成物 1

HCID 178524945HCID 178524945、化合物

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

実験手順

A solution of 3-methyl-4-phenylpyrazole (1.00 g) in tert-butanol (15 ml) and water (25 ml), at 60° C., was treated portionwise potassium permanganate (5.47 g). The temperature was then slowly elevated to 90° C. and maintained at that temperature for 5 hours. The mixture was then cooled and filtered through a pad of celite. The filtrate was concentrated and the pH was adjusted to 10 to 14 by addition of 5N aqueous sodium hydroxide solution. This mixture was washed twice with ethyl acetate. The aqueous layer was then acidified to pH 3 to 5 and then extracted four times with ethyl acetate. The combined extracts were dried over magnesium sulfate and then evaporated to yield 4-phenyl-1H-pyrazole-3-carboxylic acid (0.512 g) as a white solid, which was used without further purification. MS: 189 (M+H)+. HPLC (METHOD B): RT=2.48 minutes.

後処理

  1. customwas then slowly elevated to 90° C.
  2. temperaturemaintained at that temperature for 5 hours
  3. temperatureThe mixture was then cooled
  4. filtrationfiltered through a pad of celite
  5. concentrationThe filtrate was concentrated
  6. additionthe pH was adjusted to 10 to 14 by addition of 5N aqueous sodium hydroxide solution
  7. washThis mixture was washed twice with ethyl acetate
  8. extractionextracted four times with ethyl acetate
  9. dry with materialThe combined extracts were dried over magnesium sulfate
  10. customevaporated

出典と根拠

ORDレコード
ord-c27c744b58d74ee2ae437d88ce44abf5
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08288425B2

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