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Ethylene Glycol → HCID 59428066, 화합물

HRID 504582
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HRID 504582 반응식
[CH2:1]([O:3][C:4](=[O:19])[CH:5]([O:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[CH:17]=[O:18])[CH2:6][CH2:7][CH3:8])[CH3:2].[CH2:20](O)[CH2:21][OH:22]>C1(C)C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[CH2:1]([O:3][C:4](=[O:19])[CH:5]([O:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[CH:17]1[O:22][CH2:21][CH2:20][O:18]1)[CH2:6][CH2:7][CH3:8])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 174Ethylene GlycolHCID 594280852-(4-Chloro-2-formyl-phenoxy)-pentanoic acid ethyl ester

생성물 1

HCID 59428066HCID 59428066, 화합물수율 91.8%

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 1140Toluene용매

실험 절차

A mixture of 2-(4-chloro-2-formyl-phenoxy)-pentanoic acid ethyl ester (15 g, 53 mmol), ethylene glycol (25 mL, 440 mmol) and p-toluenesulfonic acid (0.8 g, 4.65 mmol) in toluene (150 mL) was refluxed with a Dean-Stark trap attached. After 3 h, the reaction was cooled and washed with water, saturated NaHCO3 solution and water, and the organic layer was dried over anhydrous Na2SO4 and concentrated to give the title compound as a light yellow oil (16 g).

후처리

  1. temperaturewas refluxed with a Dean-Stark trap
  2. temperaturethe reaction was cooled
  3. washwashed with water, saturated NaHCO3 solution and water
  4. dry with materialthe organic layer was dried over anhydrous Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-58820af9ba594c7c8b23c4781acfa8f8
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07776875B2

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