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2-Methoxyethanol → p-Isobutylphenylacetic acid-2-methoxyethyl ester

HRID 26460
ノート
印刷プレビュー

反応式

HRID 26460 の反応式
[CH2:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12](Cl)=[O:13])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].C(N(CC)CC)C.[CH3:22][O:23][CH2:24][CH2:25][OH:26]>>[CH3:22][O:23][CH2:24][CH2:25][O:26][C:12](=[O:13])[CH2:11][C:8]1[CH:9]=[CH:10][C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 80192-MethoxyethanolHCID 8471TriethylamineHCID 124225774-(2-Methylpropyl)benzeneacetyl chloride

生成物 1

HCID 21323304p-Isobutylphenylacetic acid-2-methoxyethyl ester収率 67.3%

実験手順

To a solution of 3.5 g of p-isobutylphenylacetic acid chloride in 5.9 g of 2-methoxyethanol was added 1.6 g of triethylamine, and the mixture was stirred at room temperature for 4 hours. After the reaction was complete, an inorganic substance produced was filtered off. The filtrate was extracted with ether, and the extract was washed, dehydrated and applied over a column of silica gel. The adsorbates was eluted with ether, and the eluates were freed of ether to give an oily product. Distillation of the product in vacuo gave 2.8 g of p-isobutylphenylacetic acid-2-methoxyethyl ester as a colorless oil, boiling at 97°-98° C./1 mmHg. Analysis-Calculated for C15H22O3 : C, 71.97; H, 8.86. Found: C, 71.63; H, 8.90. Mass spectrum: parent ion 250 m/e.

後処理

  1. customan inorganic substance produced
  2. filtrationwas filtered off
  3. extractionThe filtrate was extracted with ether
  4. washthe extract was washed
  5. washThe adsorbates was eluted with ether
  6. customto give an oily product
  7. distillationDistillation of the product in vacuo

出典と根拠

ORDレコード
ord-cdff8a6591294437abaa530021a53d05
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04150137

反応ノート

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