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

3-Chloro-1,2-propanediol → 8-(2,3-Dihydroxy)propoxy-3,4-dihydrocarbostyril

HRID 462048
ノート
印刷プレビュー

反応式

HRID 462048 の反応式
[OH-].[K+].[OH:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[NH:12][C:11](=[O:14])[CH2:10][CH2:9]2.[CH2:15]([OH:20])[CH:16]([OH:19])[CH2:17]Cl>CO>[OH:19][CH:16]([CH2:15][OH:20])[CH2:17][O:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[NH:12][C:11](=[O:14])[CH2:10][CH2:9]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 72903-Chloro-1,2-propanediolHCID 14797Potassium HydroxideHCID 2682398-Hydroxy-3,4-dihydroquinolin-2(1h)-one

生成物 1

HCID 213903498-(2,3-Dihydroxy)propoxy-3,4-dihydrocarbostyril収率 33.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

0.8 g of potassium hydroxide was dissolved in 50 ml of methanol, and 1.63 g of 8-hydroxy-3,4-dihydrocarbostyril and 1.4 g of glycerol α-monochlorohydrin were added to the resulting solution followed by refluxing the mixture for 3 hours. The raction mixture was then concentrated to dryness, and the resulting residue was extracted with 50 ml of chloroform. The extract was washed with a 2% aqueous sodium hydroxide solution and then water, and then dried over anhydrous sodium sulfate. The chloroform was then removed by distillation and the resulting residue was recrystallized from ethanol to give 0.8 g of 8-(2,3-dihydroxy)propoxy-3,4-dihydrocarbostyril as a light yellow amorphous solid having a melting point of 182° - 184° C.

後処理

  1. temperatureby refluxing the mixture for 3 hours
  2. concentrationThe raction mixture was then concentrated to dryness
  3. extractionthe resulting residue was extracted with 50 ml of chloroform
  4. washThe extract was washed with a 2% aqueous sodium hydroxide solution
  5. dry with materialwater, and then dried over anhydrous sodium sulfate
  6. customThe chloroform was then removed by distillation
  7. customthe resulting residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-9e1a08fd7f5b4c0ca324613a5ce25eb5
出典データセット
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04065456

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