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

Potassium Carbonate → HCID 53641489、化合物

HRID 330270
ノート
印刷プレビュー

反応式

HRID 330270 の反応式
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:4]([C:5](OC)=O)[C:3]=1[OH:12].[C:13]([O-])([O-])=O.[K+].[K+].Br[CH2:20][C:21]([O:23][CH3:24])=[O:22]>CC(C)=O>[CH3:13][O:12][C:3]1[C:4](=[CH:9][CH:10]=[CH:11][C:2]=1[Cl:1])[CH:5]=[CH:20][C:21]([O:23][CH3:24])=[O:22]
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 11430Potassium CarbonateHCID 60984Methyl bromoacetateHCID 104098Methyl 3-chlorosalicylate

生成物 1

HCID 53641489HCID 53641489、化合物収率 116.7%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

A mixture of 3-chlorosalicylic acid (20.2 g, 0.117 mol), Na2SO4 (5.0 g, 0.035 mol), MeOH (100 mL), and saturated methanolic HCl (40 mL) was heated under reflux for 2 days. The mixture was filtered, concentrated, and partitioned between ether and H2O. The organic phase was washed with saturated aqueous NaHCO3, dried (MgSO4) and concentrated to give a yellow oil (17.4 g). A mixture of methyl 3-chlorosalicylate (17.4 g, 0.093 mol), K2CO3 (12.9 g, 0.093 mol), and acetone (100 mL) was heated for 10 minutes. Additional acetone (100 mL) and methyl bromoacetate (14.3 g, 0.093 mol) were added and heating was continued for 18 hours. The mixture was cooled, concentrated, and partitioned between ether and H2O. The organic phase was dried (MgSO4) and concentrated to give a pale yellow oil (24.6 g, 80%).

後処理

  1. temperaturewas heated for 10 minutes
  2. temperatureheating
  3. temperatureThe mixture was cooled
  4. concentrationconcentrated
  5. custompartitioned between ether and H2O
  6. dry with materialThe organic phase was dried (MgSO4)
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-0b54c00b9c5f4f9aa38f49e476ac6f20
出典データセット
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04895860

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