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1-(2,3,6-Trifluorophenyl)ethanone → 2-(2,3,6-Trifluorophenyl)propan-2-ol

HRID 2368526
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HRID 2368526 반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([F:9])[C:3]=1[C:10](=[O:12])[CH3:11].[CH3:13][Mg]Br>C1COCC1>[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([F:9])[C:3]=1[C:10]([OH:12])([CH3:13])[CH3:11]
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참가 물질

4

반응물 2

HCID 5942471-(2,3,6-Trifluorophenyl)ethanoneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 833844992-(2,3,6-Trifluorophenyl)propan-2-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a solution of 1-(2,3,6-trifluorophenyl)ethanone (1.74 g, 10 mmol) in THF (10 mL) was added methyl magnesium bromide (7 mL, 21 mmol) at 0° C. The mixture was stirred at 0° C. for 1 hour. The reaction was quenched by addition of saturated aqueous ammonium chloride and was then extracted with EtOAc. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to afford 2-(2,3,6-trifluorophenyl)propan-2-ol. (74).

후처리

  1. customThe reaction was quenched by addition of saturated aqueous ammonium chloride
  2. extractionwas then extracted with EtOAc
  3. washThe combined organic layers were washed with water
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash column chromatography on silica gel

출처 및 근거

ORD 기록
ord-d05d134221fc4417be845ad4eeb67297
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703776B2

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