تفاعل #40580
ord-d993797223ee4d3ca68c621030b8b789
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىTemperature of the reaction liquid
- 2استخلاصfollowed by extraction with ethyl acetate
- 3غسيلThe organic layer was washed with saturated brine
- 4تجفيفdried over anhydrous sodium sulfate
- 5أخرىcondensed under reduced pressure and isopropyl ether
- 6workup.ADDITIONwas added to the resulting residue
- 7أخرىWhereupon precipitated crystals
- 8ترشيحwere recovered by filtration
الإجراء التجريبي
A solution of 2-fluoro-5-bromopyridine (7.69 g) in diethyl ether (160 ml) was cooled to −78° C., and into which n-butyl lithium (1,56M-hexane solution, 30 ml) was added dropwise at a temperature not higher than −70° C. After 15 minutes' stirring, tert-butyl 4-oxo-1-piperidinecarboxylate (8.7 g) was added. Temperature of the reaction liquid was raised to −35° C. and water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The organic layer was condensed under reduced pressure and isopropyl ether was added to the resulting residue. Whereupon precipitated crystals were recovered by filtration to provide the title compound (4.15 g). The filtrate was purified on column chromatography (hexane/ethyl acetate=3/1-2/1) to provide tert-butyl 4-(6-fluoro-3-pyridinyl)-4-hydroxy-tetrahydro-1(2H)-pyridinecarboxylate (1.25 g).