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Bis(2-bromoethyl) ether → 2,2,2-Trifluoro-1-(3-morpholin-4-yl-phenyl)-ethanone oxime

HRID 2307424
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HRID 2307424 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([C:8](=[N:13][OH:14])[C:9]([F:12])([F:11])[F:10])[CH:5]=[CH:6][CH:7]=1.Br[CH2:16][CH2:17][O:18][CH2:19][CH2:20]Br.CCN(C(C)C)C(C)C>C1(C)C=CC=CC=1>[F:10][C:9]([F:12])([F:11])[C:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([N:1]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[CH:3]=1)=[N:13][OH:14]
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참가 물질

5

반응물 3

HCID 21521Bis(2-bromoethyl) etherHCID 81531DiisopropylethylamineHCID 739856931-(3-Aminophenyl)-2,2,2-trifluoroethanone oxime

생성물 1

HCID 739856882,2,2-Trifluoro-1-(3-morpholin-4-yl-phenyl)-ethanone oxime수율 89.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 1-(3-aminophenyl)-2,2,2-trifluoroethanone oxime (1.7 g), bromoethyl ether (2.246 g), and i-Pr2NEt (2.57 g) in toluene (20 mL) was refluxed for 4 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 crude product was purified by silica gel flash chromatography (50% ethyl acetate in hexane) to give the title compound as an oil (2.04 g).

후처리

  1. temperaturewas refluxed for 4 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 crude product was purified by silica gel flash chromatography (50% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-5c57a140ed5342678bcecd7b8bbc7fd2
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831080B2

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