Hydrochloric Acid → 1-Cyclopentyl-2-phenylethan-1-one

HRID 2178101

반응식

HRID 2178101 반응식
[CH:1]1([Mg]Cl)[CH2:5][CH2:4][CH2:3][CH2:2]1.[C:8]1([CH2:14][C:15]#N)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.Cl.[O:18]1CCCC1>CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[CH:1]1([C:15](=[O:18])[CH2:14][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1

참가 물질

6

반응 조건

온도
-50 °C

실험 절차

To a solution of titanium(IV) isopropoxide (5.13 mmol, 1.46 g) in anhydrous tetrahydro-furan (10 mL) was added a solution of cyclopentylmagnesium chloride in THF (7.69 mmol) at −78° C. Reaction was warmed to −50° C. in 5 min, then maintained at that temperature for 8 min and reaction became dark-brown to black. After cooling back to −78° C., 2-phenylacetonitrile (600 mg, 5.13 mmol) was added by a syringe, and the mixture was stirred at −78° C. for 2 h. 1 N HCl aqueous solution was added to quench the reaction. The mixture was extracted with acetic acid ethyl ester (40 mL) for three times, the combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel column chromatography to give Intermediate 91 (320 mg, yield: 66.5%) as light green oil.

후처리

  1. customReaction
  2. temperaturemaintained at that temperature for 8 min
  3. customreaction
  4. temperatureAfter cooling back to −78° C.
  5. customto quench
  6. customthe reaction
  7. extractionThe mixture was extracted with acetic acid ethyl ester (40 mL) for three times
  8. washthe combined organic layer was washed with brine (30 mL)
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-4a9369f8a6994382beb308869c237b13
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09067893B2

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