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

Water → 2-(4-Ethylbenzyl)phenol

HRID 1182030
ノート
印刷プレビュー

反応式

HRID 1182030 の反応式
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16]C)=[CH:5][CH:4]=1)[CH3:2].B(Br)(Br)Br.O>ClCCl>[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[OH:16])=[CH:5][CH:4]=1)[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

5

反応物 3

HCID 962WaterHCID 25134Boron tribromideHCID 17964392(4-Ethylphenyl)(2-methoxyphenyl)methane

生成物 1

HCID 116585572-(4-Ethylbenzyl)phenol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

0.83 g of (4-ethylphenyl)(2-methoxyphenyl)methane 55 is dissolved in dichloromethane. 11.0 ml of boron tribromide (1 M in CH2Cl2) are added dropwise to the mixture. The mixture is stirred at room temperature for 5 hours and, after addition of water, the dichloromethane phase is separated off. The aqueous phase is extracted with ethyl acetate. The combined organic phases are washed with water and NaCl solution, dried over sodium sulfate and concentrated. 0.77 g is obtained as crude product which can be purified by chromatography. C15H16O (212.29) MS (ESI): 235.20 (M+Na+)

後処理

  1. customthe dichloromethane phase is separated off
  2. extractionThe aqueous phase is extracted with ethyl acetate
  3. washThe combined organic phases are washed with water and NaCl solution
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. custom0.77 g is obtained as crude product which
  7. customcan be purified by chromatography

出典と根拠

ORDレコード
ord-beda1aab79724a5890a4e1c56d86d2e5
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07288528B2

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