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

Anisole → 1-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-butene

HRID 217314
ノート
印刷プレビュー

反応式

HRID 217314 の反応式
[C:1]([O:7][C:8]1[CH:15]=[CH:14][C:11]([CH:12]=O)=[CH:10][CH:9]=1)(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].C[Si](C)(C)[CH2:18][CH:19]=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(=O)(O)[O-].[Na+].[C:34]1([O:40][CH3:41])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>[Cl-].[Hf+4].[Cl-].[Cl-].[Cl-]>[CH3:41][O:40][C:34]1[CH:39]=[CH:38][C:37]([CH:12]([C:11]2[CH:14]=[CH:15][C:8]([O:7][C:1](=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3])=[CH:9][CH:10]=2)[CH:20]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:19]=[CH2:18])=[CH:36][CH:35]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 7519Anisole2 回HCID 142474CinnamyltrimethylsilaneHCID 516892Sodium BicarbonateHCID 146834134-Formylphenyl 2,2-dimethylpropanoate

生成物 1

HCID 251119881-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-butene収率 75%

試薬・触媒・溶媒 1

HCID 9927068
Hafnium chloride (HfCl4) (6CI,8CI); Hafnium chloride; Hafnium tetrachloride; Hafnium(IV) chloride; Hafnium chloride (HfCl4), (T-4)-
触媒

実験手順

Hafnium chloride (39.2 mg, 0.122 mmol) was suspended in anisole (3, 0.02 mL) under an argon atmosphere, and then an anisole solution (0.22 mL) of 4-(pivaloyloxy)benzaldehyde (1, 25 mg, 0.121 mmol) and trimethyl cinnamylsilane (2, 46.7 mg, 0.245 mmol) was slowly added dropwise thereto under cooling by ice. The reaction mixture was stirred overnight at room temperature, then a saturated aqueous sodium bicarbonate solution (5 mL) was poured thereto, and the mixture was intensively stirred and extracted by adding diethyl ether (10 mL). The reaction mixture was further extracted two times using diethyl ether (10 mL), and then an organic layer was collected and rinsed with a saturated aqueous sodium chloride solution (5 mL), followed by drying with anhydrous magnesium sulfate and concentration thereof. The residue was purified by thin layer chromatography (hexane/methylene chloride/diethyl ether=4/1/1) to obtain the title compound as a colorless oily substance (37.7 mg, yield 75%, cin/anti mixture).

後処理

  1. temperatureunder cooling by ice
  2. stirringthe mixture was intensively stirred
  3. extractionextracted
  4. additionby adding diethyl ether (10 mL)
  5. extractionThe reaction mixture was further extracted two times
  6. customan organic layer was collected
  7. washrinsed with a saturated aqueous sodium chloride solution (5 mL)
  8. dry with materialby drying with anhydrous magnesium sulfate and concentration
  9. customThe residue was purified by thin layer chromatography (hexane/methylene chloride/diethyl ether=4/1/1)

出典と根拠

ORDレコード
ord-c5aefdce3aa74c64aa175a4a06793f4d
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193394B2

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