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

HRID 26460
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HRID 26460 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

HCID 21323304p-Isobutylphenylacetic acid-2-methoxyethyl ester수율 67.3%

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-cdff8a6591294437abaa530021a53d05
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04150137

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