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Methanol → N-[2-(benzyloxy)ethyl]-N-ethylamine

HRID 915917
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인쇄 미리보기

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HRID 915917 반응식
CS(O[CH2:6][CH2:7][O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=O)=O.CO.[CH2:18]([NH2:20])[CH3:19]>C(Cl)Cl>[CH2:9]([O:8][CH2:7][CH2:6][NH:20][CH2:18][CH3:19])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
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참가 물질

5

반응물 3

HCID 887MethanolHCID 6341EthylamineHCID 108572722-Benzyloxyethyl mesylate

생성물 1

HCID 23009168N-[2-(benzyloxy)ethyl]-N-ethylamine수율 72%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
110 °C

실험 절차

To 7.0 g (30 mmol) of 2-(benzyloxy)ethyl methanesulfonate, a 75 ml methanol solution of 2M ethylamine was added, and the mixture was heated at 110° C. in a sealed tube for 2 hours. Then, the reaction mixture was returned to room temperature, and then diluted with methylene chloride. The dilution was washed with a saturated aqueous solution of sodium hydride. The washed system was dried over sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to obtain 3.85 g (72%) of the captioned compound.

후처리

  1. customwas returned to room temperature
  2. washThe dilution was washed with a saturated aqueous solution of sodium hydride
  3. dry with materialThe washed system was dried over sodium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1)

출처 및 근거

ORD 기록
ord-f27245a924294c5ba1f41c9e527faf57
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07268128B2

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