반응 #828711
ord-8cfe8ae357454fae8802064e195ca823
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후처리
- 1기타A 500-mL round-bottom flask capped with a rubber septum, a magnetic stirring bar, and a connecting tube
- 2온도The flask was cooled in an ice bath
- 3기타Dicyclohexylborane precipitated as a white solid
- 4기타The supernatant liquid was removed by a double-ended needle
- 5세척the solid was washed with ether
- 6기타the liquid was removed
- 7기타A clear solution was obtained
- 8workup.DISTILLATIONDistillation
실험 절차
A 500-mL round-bottom flask capped with a rubber septum, a magnetic stirring bar, and a connecting tube attached to a mercury bubbler was charged with diethyl ether (150 mL) and cyclohexene (41 mL, 400 mmol). The flask was cooled in an ice bath, borane-methyl sulfide (BMS, 20 mL, 200 mmol) was added slowly, and stirring was continued for 3 h at 0° C. Dicyclohexylborane precipitated as a white solid. The supernatant liquid was removed by a double-ended needle, the solid was washed with ether, and the liquid was removed. Then the solid was suspended in 100 mL of diethyl ether, and anhydrous HCl in ether (66.7 mL of 3M solution, 200 mmol) was added slowly to the suspension at 0° C. Hydrogen is rapidly evolved and should be safely vented. A clear solution was obtained. The 11B NMR analysis of the resulting solution showed formation of Chx2BCl (δ 66 ppm in diethyl ether). Distillation provides the pure title product (δ 76 ppm in hexane), 31.6 g, 75% yield, bp 95°-96 ° C. (0.35 mm).