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

Dimethyl Sulfoxide → HCID 70606727、化合物

HRID 972088
ノート
印刷プレビュー

反応式

HRID 972088 の反応式
[CH3:1][N:2]([CH3:11])[C:3]1[C:4](C)=[CH:5][C:6](O)=[CH:7][CH:8]=1.ClC[C:14]#[N:15].[CH3:16]S(C)=O.[C:20]([O-:23])([O-])=O.[K+].[K+]>O>[CH3:11][N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][C:6]([CH3:16])=[CH:5][C:4]=1[O:23][CH2:20][C:14]#[N: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 679Dimethyl SulfoxideHCID 7856ChloroacetonitrileHCID 11430Potassium CarbonateHCID 84222Aminocarb phenol

生成物 1

HCID 70606727HCID 70606727、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

30.2 Grams of 4-dimethylamino-m-cresol and 16.0 grams of chloroacetonitrile were dissolved in 50 ml. of dimethylsulfoxide. Anhydrous K2CO3 (39.6 g) was added as a catalyst. The mixture was heated with stirring to 70°-80° C. for three hours. The reaction mixture was poured into approximately 2 liters of a ice and water mixture. The product was extracted with methylene chloride. The extract was dried with SEA SORB® and activated charcoal and the resulting mixture was filtered. The filtrate was dried under vacuum to yield 4-dimethylamino-m-tolyloxyacetonitrile.

後処理

  1. temperatureThe mixture was heated
  2. extractionThe product was extracted with methylene chloride
  3. dry with materialThe extract was dried with SEA SORB® and activated charcoal
  4. filtrationthe resulting mixture was filtered
  5. customThe filtrate was dried under vacuum

出典と根拠

ORDレコード
ord-08cdd671e4394d8baa938d5b9f1ae3b5
出典データセット
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04163105

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