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 → 6-Chloro-5-hydroxy-3,4-dihydrocarbostyril

HRID 621546
ノート
印刷プレビュー

反応式

HRID 621546 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][C:6](=[O:12])[NH:7]2.[Cl:13]Cl.O>C(O)(=O)C>[Cl:13][C:11]1[C:2]([OH:1])=[C:3]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:12])[CH2:5][CH2:4]2
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 24526ChlorineHCID 1691533,4-Dihydro-5-hydroxy-2(1H)-quinolinone

生成物 1

HCID 128994166-Chloro-5-hydroxy-3,4-dihydrocarbostyril収率 69.2%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

16.4 grams of 5-hydroxy-3,4-dihydrocarbostyril are dissolved in 300 ml of acetic acid. This solution is stirred at room temperature, and 50 ml of acetic acid solution containing 7 g of chlorine are added dropwise and the reaction is continued for 3 hours with stirring. The reaction mixture is poured into 500 ml of water and allowed to stand for 1 hour and the precipitate thus formed is separated by filtration, washed with water and then dried. Recrystallization from ethanol-water obtains 13.5 g of 6-chloro-5-hydroxy-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with a melting point of 209°-210° C.

後処理

  1. additionare added dropwise
  2. stirringwith stirring
  3. waitto stand for 1 hour
  4. customthe precipitate thus formed
  5. customis separated by filtration
  6. washwashed with water
  7. customdried
  8. customRecrystallization from ethanol-water

出典と根拠

ORDレコード
ord-dc1dd8cf247140d38e9cce63372c1a6f
出典データセット
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04824840

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