반응 #303555

ord-fa34da50d3594135831c5b413bedfab8

반응 방정식

CCOC(=O)C(F)(F)Br
ethyl bromo(difluoro)acetate
CC(=O)c1ccc(-c2ccc(F)cn2)cc1
1-[4-(5-fluoropyridin-2-yl)phenyl]ethanone
[I-].[I-].[Sm+2]
samarium diiodide
CCOC(=O)C(F)(F)C(C)(O)c1ccc(-c2ccc(F)cn2)cc1
ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the reaction was cooled
  2. 2
    기타quenched with 1N aqueous hydrochloric acid
  3. 3
    기타Volatiles were removed in vacuo
  4. 4
    기타the residue was partitioned between ethyl acetate and 1 N hydrochloric acid
  5. 5
    세척The organic phase was washed with saturated aqueous sodium bicarbonate and brine
  6. 6
    건조dried (sodium sulfate)
  7. 7
    농축concentrated in vacuo

실험 절차

A solution of ethyl bromo(difluoro)acetate (0.53 mL, 4.1 mmol) and 1-[4-(5-fluoropyridin-2-yl)phenyl]ethanone (800 mg, 3.7 mmol) in tetrahydrofuran (40 mL) was added to a 0.1 M solution of samarium diiodide in tetrahydrofuran (82 mL, 8.2 mmol) at ambient temperature. After stirring at ambient temperature for 3 min, the reaction was cooled and quenched with 1N aqueous hydrochloric acid. Volatiles were removed in vacuo and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with saturated aqueous sodium bicarbonate and brine, dried (sodium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-40% ethyl acetate/hexane afforded ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08193228B2uspto-grants-2012_06