반응 #569177

ord-5d4d976024f048d5933294c8240db91f

반응 방정식

Cl
Hydrochloric acid
O=C1CN2CCC1CC2
quinuclidin-3-one
[Li][CH](C)CC
sec-butyllithium
Brc1ccc(-c2ccccc2)cc1
4-bromobiphenyl
OC1(c2ccc(-c3ccccc3)cc2)CN2CCC1CC2
3-(biphenyl-4-yl)-3-hydroxyquinuclidine
수율 41.1%

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGStirring
  2. 2
    workup.WAITwas continued at -78° C. for 30 minutes
  3. 3
    workup.WAITto reach room temperature over 2 hours
  4. 4
    기타the reaction temperature below 10° C
  5. 5
    기타The aqueous layer was separated
  6. 6
    세척washed with diethyl ether (2×300 ml) before the addition of excess sodium hydroxide solution (density 1.35 g/cm3) to pH14
  7. 7
    추출The mixture was extracted with ethyl acetate which
  8. 8
    기타the ethyl acetate phase separated
  9. 9
    건조dried (Na2SO4)
  10. 10
    기타evaporated
  11. 11
    기타to yield a colourless solid which
  12. 12
    기타crystallised from ethyl acetate

실험 절차

A solution of sec-butyllithium in cyclohexane (100 ml, 1.3M) was added dropwise with stirring to a solution of 4-bromobiphenyl (25 g) in dry tetrahydrofuran (240 ml) under an argon atmosphere at -78° C. The mixture was stirred for 5 minutes and a solution of quinuclidin-3-one (12 g) in dry tetrahydrofuran (100 ml) added during 20 minutes. Stirring was continued at -78° C. for 30 minutes and the mixture allowed to reach room temperature over 2 hours. 2M Hydrochloric acid (225 ml) was added keeping the reaction temperature below 10° C. The aqueous layer was separated and washed with diethyl ether (2×300 ml) before the addition of excess sodium hydroxide solution (density 1.35 g/cm3) to pH14. The mixture was extracted with ethyl acetate which had been heated to 50° C. and the ethyl acetate phase separated, dried (Na2SO4) and evaporated to yield a colourless solid which crystallised from ethyl acetate to give 3-(biphenyl-4-yl)-3-hydroxyquinuclidine (11.0 g) m.p. 165°-166° C.; microanalysis, found: C, 81.1; H, 7.5; N, 5.2%; C19H21NO 0.1H2O requires: C, 81.1; H, 7.5; N, 5.0%; NMR (CDCl3 /CD3CO2D): 1.7-1.9(3H, m,), 2.5(1H, m), 2.5-2.7(1H, m), 3.2-3.5(4H, m), 3.7(1H, dd), 4.0(1H, dd) and 7.3-7.7(9H, m); m/z 279 (M+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05792777uspto-grants-1998_08