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

Imidazole → 4-(2-Iodoethyl)phenol

HRID 133777
ノート
印刷プレビュー

反応式

HRID 133777 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:25]I.[OH:27][C:28]1[CH:36]=[CH:35][C:31]([CH2:32][CH2:33]O)=[CH:30][CH:29]=1.I.N1C=CN=C1>O.ClCCl>[I:25][CH2:33][CH2:32][C:31]1[CH:35]=[CH:36][C:28]([OH:27])=[CH:29][CH:30]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 795Imidazole2 回HCID 807IodineHCID 11776TriphenylphosphineHCID 86760696HCID 86760696、化合物

生成物 1

HCID 2456964-(2-Iodoethyl)phenol

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344
Dichloromethane
溶媒

実験手順

Triphenylphosphine (1.57 g, 0.006 mol) and imidazole (0.41 g, 0.006 mol) were added to dry dichloromethane (20 ml). When the imidazole was in solution iodine (1.52 g, 0.006 mol) was added. After precipitation of the imidazole hydroiodide (4-hydroxyphenethyl) alcohol (0.69 g, 0.005 mol) was added. The mixture was stirred at room temperature for 4 h. Then water was added and the mixture was extracted with dichloromethane. The extracts were washed with water, dried and concentrated in vacuo to give a raw product. Purification by flash chromatography (heptane/ethyl acetate as a gradient eluent 9:1-6:4) gave a pure product. 1H NMR (400 MHz, DMSO-d6): 2.99 (2H, t, 3J=7.6 Hz), 3.38 (2H, t, 3J=7.6 Hz), 6.68 (2H, d, 3J=8.5 Hz), 7.03 (2H, d, 3J=8.5 Hz), 9.24 (1H, s, —OH).

後処理

  1. additionwas added
  2. additionwas added
  3. extractionthe mixture was extracted with dichloromethane
  4. washThe extracts were washed with water
  5. customdried
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2ee50908e1a44115932157e000847182
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07390923B2

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