반응 #9891

ord-1e3ad5c77d6a4913a7de709d2d308fb0

반응 방정식

O=C1CCC(=O)N1Br
NBS
C=CCCCCCCCCO
dec-9-en-1-ol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
C=CCCCCCCCCBr
10-bromo-dec-1-ene
수율 81.0%

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the reaction was quenched with methanol (0.8 mL)
  2. 2
    workup.ADDITIONThe solution was diluted with ether (80 mL)
  3. 3
    세척washed with water, saturated aqueous NaHCO3 and brine successively
  4. 4
    기타The organic layer was dried
  5. 5
    농축concentrated
  6. 6
    기타The residue was purified by flash chromatography on silica gel
  7. 7
    세척eluting with hexane

실험 절차

To a solution of dec-9-en-1-ol (1.22 g, 7.82 mmol) in DMF (18 mL) was added triphenylphosphine (2.30 g, 8.77 mmol). The solution was cooled to 0° C. and NBS (1.52 g, 8.54 mmol) was added in portions. After stirring for 30 min at room temperature, the reaction was quenched with methanol (0.8 mL). The solution was diluted with ether (80 mL), washed with water, saturated aqueous NaHCO3 and brine successively. The organic layer was dried and concentrated. The residue was purified by flash chromatography on silica gel, eluting with hexane to afford 10-bromo-dec-1-ene (1.38 g, 81%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.80 (1H, m), 4.94 (2H, m), 3.38 (2H, t, J=6.9 Hz), 2.02 (2H, m), 1.83 (2H, m), 1.20–1.55 (10H, m); 13C NMR (75 MHz, CDCl3) δ 139.17, 114.30, 34.29, 34.02, 33.06, 29.53, 29.25, 29.12, 28.96, 28.40.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091357B2uspto-grants-2006_08