反应详情

Prepared using methodology described by Zaragoza, F., et al. J. Med. Chem. 2004, 47, 2833. To a stirred mixture of diethylamine (10.3 mL, 99.6 mmol), 3-chloro-3-methylbut-1-yne (10.2 g, 99.6 mmol), triethylamine (16.7 mL, 119 mmol), and THF (100 mL) at 0° C. was added copper(I) chloride (0.986 g, 9.96 mmol). The resulting suspension was allowed to warm to room temperature, and stirring continued for 4 hours. The reaction mixture was partitioned between diethyl ether (250 mL) and a saturated aqueous solution of NaHCO3 (100 mL). The phases were separated, and the aqueous phase was re-extracted with diethyl ether (100 mL). The combined organic phases were dried (Na2SO4), filtered, and concentrated. The brown oil was distilled (105-110° C.) at atmospheric pressure under N2. The product was obtained as an oil (1.85 g, 9%). 1H NMR (400 MHz, CDCl3) δ 2.66 (q, J=7 Hz, 4H), 2.21 (s, 1H), 1.40 (s, 6H), 1.08 (t, J=7 Hz, 6H).

1. customPrepared
2. customThe reaction mixture was partitioned between diethyl ether (250 mL)
3. customThe phases were separated
4. extractionthe aqueous phase was re-extracted with diethyl ether (100 mL)
5. dry with materialThe combined organic phases were dried (Na2SO4)
6. filtrationfiltered
7. concentrationconcentrated
8. distillationThe brown oil was distilled (105-110° C.) at atmospheric pressure under N2