Реакция #1126972
ord-650b5673bee745408ce898282a79d73b
Уравнение реакции
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Условия реакции
Обработка
- 1Фильтрацияbefore filtering the suspension through celite in vacuo
- 2ПромывкаThe filter cake was washed with diethyl ether (60 mL)
- 3workup.ADDITIONHydrochloric acid (1M, 60 mL) was added to the filtrate
- 4Другоеthe organic phase separated
- 5ЭкстракцияThe aqueous layer was extracted with diethyl ether (60 mL)
- 6Промывкаthe combined organic phase was washed with brine (60 mL)
- 7Сушкаdried (MgSO4)
- 8Фильтрацияfiltered
- 9workup.DISSOLUTIONThe residue was dissolved in ammonium hydroxide (18 mL)
- 10Другоеthe solvents were removed in vacuo
- 11ДругоеThe residue was azeotroped with diethyl ether (3×10 mL)
Методика
A solution of ammonium chloride (600 mg, 11.2 mmol) in water (7.5 mL) was added to a solution of bromotosylate (47) (3.0 g, 8.26 mmol) in propan-2-ol (15 mL) under argon. Zinc dust (600 mg, 9.2 mmol) was then added in portions over 4 minutes and the mixture was stirred for 16 hours before filtering the suspension through celite in vacuo. The filter cake was washed with diethyl ether (60 mL). Hydrochloric acid (1M, 60 mL) was added to the filtrate then the organic phase separated. The aqueous layer was extracted with diethyl ether (60 mL) then the combined organic phase was washed with brine (60 mL), then dried (MgSO4), filtered and reduced in vacuo. The residue was dissolved in ammonium hydroxide (18 mL) and a solution of ammonia in propan-2-ol (12 mL, 2.0M, 24 mmol), then divided into two equal portions and heated in sealed tubes at 75° C. for 16 hours. The mixtures were combined using methanol then the solvents were removed in vacuo. The residue was azeotroped with diethyl ether (3×10 mL) to obtain (R)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol which was used without further purification.