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Bis(2-bromoethyl) ether → 1-(2-Fluoro-5-morpholin-4-yl-phenyl)ethanone

HRID 2307429
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HRID 2307429 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1.Br[CH2:13][CH2:14][O:15][CH2:16][CH2:17]Br.CCN(C(C)C)C(C)C>C1(C)C=CC=CC=1>[F:11][C:5]1[CH:4]=[CH:3][C:2]([N:1]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)=[CH:7][C:6]=1[C:8](=[O:10])[CH3:9]
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참가 물질

5

반응물 3

HCID 21521Bis(2-bromoethyl) etherHCID 81531DiisopropylethylamineHCID 27811251-(5-Amino-2-fluorophenyl)ethanone

생성물 1

HCID 226054681-(2-Fluoro-5-morpholin-4-yl-phenyl)ethanone수율 73.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 1-(5-amino-2-fluoro-phenyl)-ethanone (3.5 g), bromoethyl ether (5.929 g), and i-Pr2NEt (7.121 g) in toluene (20 mL) was refluxed for 16 hours. After cooling, the reaction mixture was quenched with water. The aqueous layer was extracted with dichloromethane, and the combined organic layers were dried over magnesium sulphate, filtered, and concentrated in vacuo. The residue was purified by silica gel flash chromatography (25% ethyl acetate in hexane) to give 3.74 g of the title compound as an oil.

후처리

  1. temperaturewas refluxed for 16 hours
  2. temperatureAfter cooling
  3. customthe reaction mixture was quenched with water
  4. extractionThe aqueous layer was extracted with dichloromethane
  5. dry with materialthe combined organic layers were dried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by silica gel flash chromatography (25% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-741a641706fa49c083d8dcf5d9da262f
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831080B2

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