Реакция #2348085
ord-9e78c93bde7f467e939d2519372aec94
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.WAITthe stirring was continued for additional 180 minutes
- 2ДругоеThe resulting reaction mixture
- 3Другоеto come to 0° C.
- 4workup.ADDITIONpoured into a vessel
- 5Температураhad been chilled at 0° C.
- 6workup.ADDITIONmixed
- 7Другоеto be separated into an organic layer
- 8ЭкстракцияExtraction
- 9ПромывкаThe extracts were washed with brine
- 10Сушкаdried over anhydrous magnesium sulfate
- 11workup.DISTILLATIONThen, the solvent was distilled off under reduced pressure
Методика
The compound (T17) and THF (1,000 ml) were put into a reaction vessel under an atmosphere of nitrogen, and chilled to −71° C. Then, a sec-butyl lithium solution (1.0 M in cyclohexane and n-hexane; 1,000 ml) were added dropwise thereto in the temperature range of −71° C. to −62° C., and the stirring was continued for additional 120 minutes. Subsequently, trimethyl borate (127.6 g) was added dropwise in the temperature range of −70° C. to −59° C., and the stirring was continued for additional 180 minutes. The resulting reaction mixture was allowed to come to 0° C., and then poured into a vessel containing 1N-hydrochloric acid (3,000 ml) and ethyl acetate (3,000 ml) which had been chilled at 0° C. and mixed. The mixture was then allowed to stand to be separated into an organic layer and an aqueous layer. Extraction was carried out and the resulting organic layer was fractionated. The extracts were washed with brine, and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, whereby 115.9 g of phenylboronic acid derivative (T18) was obtained.