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

HRID 1926574
ノート
印刷プレビュー

反応式

HRID 1926574 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.O.C(=O)(O)[O-].[Na+].[CH2:35]([O:37][CH2:38][CH3:39])C>C1(OC)C=CC=CC=1.[Cl-].[Hf+4].[Cl-].[Cl-].[Cl-]>[CH3:35][O:37][C:38]1[CH:39]=[CH:10][C:9]([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:8][CH:15]=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 3283Diethyl EtherHCID 142474CinnamyltrimethylsilaneHCID 146834134-Formylphenyl 2,2-dimethylpropanoateHCID 86585896Sodium bicarbonate water

生成物 1

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

試薬・触媒・溶媒 2

HCID 9927068
Hafnium chloride (HfCl4) (6CI,8CI); Hafnium chloride; Hafnium tetrachloride; Hafnium(IV) chloride; Hafnium chloride (HfCl4), (T-4)-
触媒
HCID 7519Anisole溶媒2 回

実験手順

Under an argon atmosphere, hafnium chloride (39.2 mg, 0.122 mmol) is suspended in anisole (3, 0.02 mL), and under ice cooling, an anisole (0.22 mL) solution of 4-(pivaloyloxy)benzaldehyde (1, 25 mg, 0.121 mmol) and trimethylcinnamylsilane (2, 46.7 mg, 0.245 mmol) was slowly added dropwise. After stirring overnight at room temperature, saturated sodium bicarbonate water (5 mL) was poured into the reaction mixture with vigorous stirring, diethyl ether (10 mL) was added and extraction was performed. Extractions were further carried out two times with diethyl ether (10 mL), the organic layers were combined, washed with a saturated sodium chloride aqueous solution (5 mL), dried with anhydrous magnesium sulfate, and concentrated. The residue was purified by thin layer chromatography (hexane:methylene chloride:diethyl ether=4:1:1), and the subject compound (4, 37.7 mg) was obtained as a colorless oily substance (yield 75%, syn/anti mixture).

後処理

  1. additionwas added
  2. extractionextraction
  3. extractionExtractions
  4. washwashed with a saturated sodium chloride aqueous solution (5 mL)
  5. dry with materialdried with anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customThe residue was purified by thin layer chromatography (hexane:methylene chloride:diethyl ether=4:1:1)
  8. customthe subject compound (4, 37.7 mg) was obtained as a colorless oily substance (yield 75%, syn/anti mixture)

出典と根拠

ORDレコード
ord-229e7c4452d643f5bf3d904a69ab9b34
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183235B2

反応ノート

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