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

Sodium Hydroxide → 8-Bromo-3-methyl-5,6,7,8-tetrahydroquinoline

HRID 649175
ノート
印刷プレビュー

反応式

HRID 649175 の反応式
[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6](O)[CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1.P(Br)(Br)[Br:14].[OH-].[Na+]>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6]([Br:14])[CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=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 14798Sodium HydroxideHCID 24614Phosphorus tribromideHCID 123582223-Methyl-5,6,7,8-tetrahydroquinolin-8-ol

生成物 1

HCID 139602608-Bromo-3-methyl-5,6,7,8-tetrahydroquinoline

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

1.50 Grams of 3-methyl-8-hydroxy-5,6,7,8-tetrahydroquinoline was dissolved in 20 ml of chloroform, to this solution was added dropwise a solution consisting of 1.35 g of phosphorus tribromide and 5 ml of chloroform under ice-cooled condition, then the mixture was stirred under ice-cooled condition for 2 hours, next was stirred at room temperature overnight. To the reaction mixture was added 5%-sodium hydroxide aqueous solution, then was extracted with chloroform. The chloroform layer was washed with an aqueous solution saturated with sodium chloride, and dried with anhydrous magnesium sulfate. The solvent was removed by evaporation to obtain 1.80 g of 3-methyl-8-bromo-5,6,7,8-tetrahydroquinoline.

後処理

  1. additionwas added dropwise a solution
  2. temperaturecooled condition
  3. temperaturecooled condition for 2 hours
  4. stirringnext was stirred at room temperature overnight
  5. extractionwas extracted with chloroform
  6. washThe chloroform layer was washed with an aqueous solution saturated with sodium chloride
  7. dry with materialdried with anhydrous magnesium sulfate
  8. customThe solvent was removed by evaporation

出典と根拠

ORDレコード
ord-ba5ce626a49346099c909ad07942421c
出典データセット
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04738970

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