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Diethyl Ether → 2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanone

HRID 858682
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HRID 858682 반응식
CO[Mg][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Br-].[F:11][C:12]([F:18])([F:17])[C:13](OC)=[O:14].[CH2:19]([O:21]CC)C>>[F:11][C:12]([F:18])([F:17])[C:13]([C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:9]=1[O:21][CH3:19])=[O:14]
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참가 물질

4

반응물 3

HCID 3283Diethyl EtherHCID 9893Methyl trifluoroacetateHCID 178502596HCID 178502596, 화합물

생성물 1

HCID 27597332,2,2-Trifluoro-1-(2-methoxyphenyl)ethanone

실험 절차

2 Methoxy Phenyl magnesium bromide (35 ml) was added slowly to a solution of methyl trifluoroacetate (5.0 g) in diethyl ether (100 ml) @ −78° C. The reaction mixture was warmed to room temperature over 12 hrs and the quenched with saturated ammonium chloride solution (100 ml). The mixture was then partitioned between ethyl acetate (500 ml) and water (250 ml) The organics were separated and dried over magnesium sulfate filtered and concentrated in vacuuo. The crude residue was purified by column chromatography on silica gel eluting with 100% hexanes, 90:10 and 80:20, hexanes:ethyl acetate, to afford title compound as a yellow oil. (4.0 g). 1H NMR (CDCl3): δ 3.57 (s, 3H), 7.00 (m, 2H), 7.35 (m, 1H), 7.63, (d, J=2.54 Hz 2H).

후처리

  1. customthe quenched with saturated ammonium chloride solution (100 ml)
  2. customThe mixture was then partitioned between ethyl acetate (500 ml) and water (250 ml) The
  3. customorganics were separated
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuuo
  7. customThe crude residue was purified by column chromatography on silica gel eluting with 100% hexanes, 90:10 and 80:20, hexanes

출처 및 근거

ORD 기록
ord-1628f31895ca4825ba6c8013fac50920
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07148226B2

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