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

Ethyl-3-(5'-fluoro-2'-methoxybenzyl)acrylate → Ethyl-4-(5'-fluoro-2'-methoxyphenyl)butyrate

HRID 1919518
ノート
印刷プレビュー

反応式

HRID 1919518 の反応式
[CH2:1]([O:3][C:4](=[O:17])[CH:5]=[CH:6][CH2:7][C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[CH:10][C:9]=1[O:15][CH3:16])[CH3:2]>C(O)C.[Pd]>[CH2:1]([O:3][C:4](=[O:17])[CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[CH:10][C:9]=1[O:15][CH3:16])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 67499893Ethyl-3-(5'-fluoro-2'-methoxybenzyl)acrylate

生成物 1

HCID 67499284Ethyl-4-(5'-fluoro-2'-methoxyphenyl)butyrate収率 95%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of ethyl-3-(5′-fluoro-2′-methoxybenzyl)acrylate (2.36 g, 10.0 mmol) in ethanol (100%, 40 mL) under Ar(g) was added Pd/C (10%, 200 mg) very carefully and the flask containing the mixture was evacuated and purged with H2 three time each. Then a balloon was attached to the flask and the reaction was allowed to go for 15 h at room temperature. The reaction mixture was filtered through a pad of silica eluted with mixed solvent of EtOAc and Hexane (1:1). The crude product that obtained by removal of the solvent in vacuo was purified by a flash column chromatography (10% EtOAc in hexane, Rf=0.20) to give the product (2.25 g, 95%).

後処理

  1. additionthe flask containing the mixture
  2. customwas evacuated
  3. custompurged with H2 three time each
  4. filtrationThe reaction mixture was filtered through a pad of silica
  5. washeluted with mixed solvent of EtOAc and Hexane (1:1)
  6. customThe crude product that obtained by removal of the solvent in vacuo
  7. customwas purified by a flash column chromatography (10% EtOAc in hexane, Rf=0.20)

出典と根拠

ORDレコード
ord-be14934034144929a1b44daa136a13e2
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08168635B2

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