反应 #62885
ord-f62e782a7f304355a72a847c680ab3d5
反应方程式
反应物
试剂
反应条件
后处理
- 1workup.ADDITIONcopper (I) bromide - dimethyl sulphide complex (1.54 g) was added in one portion
- 2温度to warm to 0° C., for a period of 15 minutes
- 3温度After cooling to -70° C.
- 4workup.ADDITIONwas added to the reaction mixture, which
- 5萃取was then extracted with ethyl acetate
- 6其他After drying
- 7其他the solvent was evaporated under reduced pressure
- 8其他to give an orange oil
- 9洗涤eluting with petroleum ether (boiling range 40°-60° C.)
- 10workup.ADDITIONcontaining diethyl ether (5% by volume)
实验过程
n-Butyl lithium (2.5 M in hexane, 3 cm3) was added portionwise to a solution of 2-[4-bromo-2,3,5,6-tetrafluorobenzyloxy]-tetrahydropyran (1.7 g) in dry tetrahydrofuran (10 cm3) under an atmosphere of dry nitrogen, whilst the reaction temperature was maintained at -70° C. After 30 minutes, copper (I) bromide - dimethyl sulphide complex (1.54 g) was added in one portion and the reaction temperature allowed to warm to 0° C., for a period of 15 minutes. After cooling to -70° C., a solution of Z-1-chloro-3-iodoprop-1-ene (2.03 g) in dry tetrahydrofuran (3 cm3) was added portionwise, and the reaction mixture stirred for a further hour at -70° C. After warming to the ambient temperature, (ca. 25° C.), aqueous ammonium chloride was added to the reaction mixture, which was then extracted with ethyl acetate. After drying, the solvent was evaporated under reduced pressure to give an orange oil. The residue was then subjected to medium pressure column chromatography on a silica gel column using a Gilson apparatus, eluting with petroleum ether (boiling range 40°-60° C.) containing diethyl ether (5% by volume) to give 2-[4-(3-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyloxy]-tetrahydropyran, as a mixture consisting predominantly of the Z isomer.