5-Chloro-2-fluorobenzaldehyde → HCID 83988321, 화합물

HRID 468880

반응식

HRID 468880 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([F:10])=[C:6]([CH:9]=1)[CH:7]=[O:8].[CH2:11]([Mg]Br)[CH3:12]>C(OCC)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([F:10])=[C:6]([CH:7]([OH:8])[CH2:11][CH3:12])[CH:9]=1

참가 물질

4

반응 조건

온도
0 °C

실험 절차

To a solution of 5-chloro-2-fluorobenzaldehyde (1 g, 6.3 mmol) in diethyl ether (20 mL) cooled at −78° C. was added a solution of 3.0M ethylmagnesium bromide in ether (4.2 mL, 13 mmol) dropwise over 5 minutes. The reaction mixture was warmed to 0° C. and after 30 minutes was quenched with a few drops of saturated aqueous ammonium chloride solution. The reaction mixture was diluted with ethyl acetate (50 mL) and washed with water (50 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 4 g, ISCO, 0-30% ethyl acetate in heptane) to afford the title compound as a pale yellow oil (850 mg, 71%), which was used in the next step without further purification.

후처리

  1. customwas quenched with a few drops of saturated aqueous ammonium chloride solution
  2. additionThe reaction mixture was diluted with ethyl acetate (50 mL)
  3. washwashed with water (50 mL)
  4. customThe organic layer was separated
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customto afford a residue that
  9. customwas purified by flash chromatography (silica, 4 g, ISCO, 0-30% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-8ffec19b8ae9416ba1b9d93536591c21
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08623889B2

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