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Diethyl Ether → (1-Ethylcyclohexyl)acetaldehyde

HRID 1820315
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반응식

HRID 1820315 반응식
C(O)(=O)C.C(O)(=O)C.IC1C=CC=CC=1.[CH2:16]([C:18]1([CH2:24][CH2:25][OH:26])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)[CH3:17].CC1(C)N([O])C(C)(C)CCC1.C(OCC)C>C(Cl)Cl>[CH2:16]([C:18]1([CH2:24][CH:25]=[O:26])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1)[CH3:17]
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참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 2724126TempoHCID 12217721Iodo benzene diacetateHCID 231099022-(1-Ethylcyclohexyl)ethanol

생성물 1

HCID 45091813(1-Ethylcyclohexyl)acetaldehyde수율 220.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

After adding iodobenzene diacetate (1.61 g, 4.98 mmol) to a solution of 2-(1-ethylcyclohexyl)ethanol (708 mg, 4.53 mmol) in methylene chloride (15 mL) at room temperature, 2,2,6,6-tetramethylpiperidine 1-oxyl free radical (70.8 mg, 0.450 mmol) was added and the mixture was stirred for 15 hours. Diethyl ether was added to the reaction mixture, which was then washed with 10% aqueous sodium thiosulfate, 1N hydrochloric acid and saturated aqueous sodium hydrogencarbonate in that order. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to obtain the title compound as an orange oil (1.54 g).

후처리

  1. washwas then washed with 10% aqueous sodium thiosulfate, 1N hydrochloric acid and saturated aqueous sodium hydrogencarbonate in that order
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-adbc7d5bb83a4ccba4c03f9e2bdb21e3
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07601843B2

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