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

Acetone → 3,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcohol

HRID 322606
ノート
印刷プレビュー

反応式

HRID 322606 の反応式
[CH:1]([C:3]1[CH:28]=[CH:27][C:6]([CH2:7][O:8][C:9]2[CH:10]=[C:11]([CH:14]=[C:15]([O:17][CH2:18][C:19]3[CH:24]=[CH:23][C:22]([CH:25]=[CH2:26])=[CH:21][CH:20]=3)[CH:16]=2)[CH2:12]Br)=[CH:5][CH:4]=1)=[CH2:2].[CH3:29][C:30]([CH3:32])=[O:31].[OH:33][C:34]1[CH:35]=[C:36]([CH:39]=[C:40]([OH:42])[CH:41]=1)[CH2:37][OH:38].[C:43]([O-:46])([O-])=O.[K+].[K+]>C1(C)C=CC=CC=1.CCCCCC.O.C(Cl)Cl>[CH:1]([C:3]1[CH:28]=[CH:27][C:6]([CH2:7][O:8][C:9]2[CH:10]=[C:11]([CH:14]=[C:15]([O:17][CH2:18][C:19]3[CH:24]=[CH:23][C:22]([CH:25]=[CH2:26])=[CH:21][CH:20]=3)[CH:16]=2)[CH2:12][O:31][C:30]2[CH:32]=[C:16]([CH:9]=[C:10]([O:38][CH2:37][C:36]3[CH:35]=[C:34]([O:33][CH2:18][C:19]4[CH:24]=[CH:23][C:22]([CH:25]=[CH2:26])=[CH:21][CH:20]=4)[CH:41]=[C:40]([O:42][CH2:7][C:6]4[CH:5]=[CH:4][C:3]([CH:1]=[CH2:2])=[CH:28][CH:27]=4)[CH:39]=3)[CH:29]=2)[CH2:43][OH:46])=[CH:5][CH:4]=1)=[CH2:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 180AcetoneHCID 11430Potassium CarbonateHCID 346613,5-Dihydroxybenzyl alcoholHCID 184339453,5-Bis(4-vinylbenzyloxy)benzyl bromide

生成物 1

HCID 184339443,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcohol収率 81.9%

試薬・触媒・溶媒 4

HCID 962
Water
溶媒
HCID 1140Toluene溶媒
HCID 6344Dichloromethane溶媒
HCID 8058Hexane溶媒

実験手順

A 250 ml flask is charged with 15 g (34.5 mmol, 2.2 eq) of bromide (2) and acetone (100 ml) under an argon atmosphere. To this solution is added 3,5-dihydroxybenzyl alcohol (2.2 g, 15.7 mmol), 0.82 g (31. mmol, 0.2 eq) 18-C-6 and 4.77 g (34-5 mmol, 2.2 eq) of K2CO3 and the mixture is stirred for 48 hours whereupon a yellow suspension is formed. To the mixture is added methylene chloride (200 ml) and water (200 ml). The organic phase is separated, dried over MgSO4 and evaporated to dryness. A dark brown oil is obtained which is dissolved in toluene (40 ml) and hexane (20 ml). Upon cooling, a white powder forms which is collected by filtration to give 10.92 g (81.9% of (3A).

後処理

  1. customis formed
  2. customThe organic phase is separated
  3. dry with materialdried over MgSO4
  4. customevaporated to dryness
  5. customA dark brown oil is obtained which
  6. temperatureUpon cooling
  7. filtrationa white powder forms which is collected by filtration

出典と根拠

ORDレコード
ord-7c38a8d86c804a088e9b4407bbaf07ed
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06211316B1

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