HRID1008848

反应详情

EQUATION

反应方程式

HRID 1008848 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

A solution (0.45 M) of the preceding compound in hexane was treated with a solution (15%) of Et2Zn (1.2 eq) in toluene, and the resulting solution was cooled in an ice bath. Diiodomethane (1.2 eq) was added dropwise, then the solution was stirred for 1 h before being warmed to 20° C. Pyridine (6 eq) was added, and the slurry was stirred for 15 min then poured onto petroleum ether. The mixture was filtered repeatedly through CELITE until a transparent solution was obtained. This mixture was concentrated at 100 mbar, and the solution that remained (that contained trimethyl{[(trans)-2-pent-4-en-1-ylcyclopropyl]oxy}silane, toluene and pyridine) was further diluted with THF. The mixture was cooled to 0° C. then treated dropwise with a solution (1 M) of TBAF (1.2 eq) in THF. After 10 min, the mixture was allowed to warm to 20° C., and after a further 1 h was poured into H2O. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed with brine then dried. Removal of the volatiles afforded a residue that was purified by flash chromatography (eluent 0-66% Et2O/petroleum ether) to furnish the title compound (71%) as a colorless liquid. 1H NMR (400 MHz, CDCl3) δ 5.85-5.75 (m, 1H), 5.00 (dd, J=17.1, 1.6 Hz, 1H), 4.94 (br d, J=10.4 Hz, 1H), 3.20 (apparent dt, J=6.4, 2.5 Hz, 1H), 2.10-2.04 (m, 2H), 1.52-1.44 (m, 2H), 1.29-1.19 (m, 1H), 1.15-1.07 (m, 1H), 0.95-0.87 (m, 1H), 0.71-0.66 (m,1H), 0.31 (apparent q, J=6.0 Hz, 1H).

WORKUP

后处理

  1. temperaturethe resulting solution was cooled in an ice bath
  2. stirringthe slurry was stirred for 15 min
  3. additionthen poured onto petroleum ether
  4. filtrationThe mixture was filtered repeatedly through CELITE until a transparent solution
  5. customwas obtained
  6. concentrationThis mixture was concentrated at 100 mbar
  7. additionwas further diluted with THF
  8. temperatureThe mixture was cooled to 0° C.
  9. waitAfter 10 min
  10. temperatureto warm to 20° C.
  11. extractionThe aqueous phase was extracted with EtOAc
  12. washthe combined organic extracts were washed with brine
  13. customthen dried
  14. customRemoval of the volatiles
  15. customafforded a residue that
  16. customwas purified by flash chromatography (eluent 0-66% Et2O/petroleum ether)