Benzyl Bromide → Benzyl propiolate

HRID 243704노트

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HRID 243704 반응식
[C:1]([OH:5])(=[O:4])[C:2]#[CH:3].[CH2:6](Br)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C>[C:1]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:4])[C:2]#[CH:3]

참가 물질

5

실험 절차

To a solution of 17.0 g (233 mmol) of propiolic acid in 600 mL of anhydrous DMF was added 39.9 g (233 mmol) of benzyl bromide followed by portionwise addition of 76.0 g (233 mmol) of Cs2CO3. After stirring at room temperature for 24 h, the reaction was quenched with a saturated aqueous ammonium chloride solution and extracted with EtOAc (3×200 mL). The combined extracts were washed with water then brine and dried over anhydrous sodium sulfate. The mixture was then filtered through a silica gel pad washing with hexanes, and the filtrate was evaporated under reduced pressure to afford a crude product. The crude product was purified by silica gel chromatography eluting with a 0-20% ethyl acetate in hexane gradient to afford the title compound as a colorless oil (13.8 g, 35%). 1H NMR (CDCl3, 500 MHz) δ 7.41 (m, 5H), 5.25 (s, 2H), 2.92 (s, 1H).

후처리

  1. customthe reaction was quenched with a saturated aqueous ammonium chloride solution
  2. extractionextracted with EtOAc (3×200 mL)
  3. washThe combined extracts were washed with water
  4. dry with materialbrine and dried over anhydrous sodium sulfate
  5. filtrationThe mixture was then filtered through a silica gel pad
  6. washwashing with hexanes
  7. customthe filtrate was evaporated under reduced pressure
  8. customto afford a crude product
  9. customThe crude product was purified by silica gel chromatography
  10. washeluting with a 0-20% ethyl acetate in hexane gradient

출처 및 근거

ORD 기록
ord-57851859c4324cf18eba98e52226e682
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08653260B2

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