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

Hydrochloric Acid → Methyl 2,4,5-trimethylphenylacetate

HRID 853736
ノート
印刷プレビュー

反応式

HRID 853736 の反応式
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH2:10][C:11]([OH:13])=[O:12].Cl.[CH3:15]O>>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH2:10][C:11]([O:13][CH3:15])=[O:12]
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 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 2989242-(2,4,5-Trimethylphenyl)acetic acid

生成物 1

HCID 22336857Methyl 2,4,5-trimethylphenylacetate

実験手順

100 g (0.56 mol) of 2,4,5-trimethylphenylacetic acid were dissolved in 230 ml of methanol, 6 ml of concentrated hydrochloric acid were added and the mixture was heated under reflux for 10 hours. It was then cooled to room temperature and the methanol was removed in vacuo. The residue was stirred into a solution of 53 g of sodium carbonate, dissolved in 260 ml of water, and the organic phase was taken up in 200 ml of toluene. The organic phase was separated off, dried and concentrated and the residue was distilled. 48.6 g of methyl 2,4,5-trimethylphenylacetate having a boiling point of 86° C. under 0.2 mbar were obtained.

後処理

  1. temperature
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
the mixture was heated
  • temperatureunder reflux for 10 hours
  • customthe methanol was removed in vacuo
  • dissolutiondissolved in 260 ml of water
  • customThe organic phase was separated off
  • customdried
  • concentrationconcentrated
  • distillationthe residue was distilled
  • 出典と根拠

    ORDレコード
    ord-13cdd28ed1b34359b34aca17c0faa4dd
    出典データセット
    uspto-grants-2007_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07256158B2

    反応ノート

    読み込み中…