Method for preparing 1,3-dimethyladamantane
A technology of dimethyladamantane and dibromoadamantane, applied in 1 field, can solve problems such as being unsuitable for industrial production, and achieve the effects of improving product purity and mild process conditions
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Embodiment 1
[0028] Add 1.1 mL (1.72 g, 11 mmol) of titanium tetrachloride and 0.13 g (1 mmol) of titanium trichloride to 100 mL of dimethylzinc (1M) in dichloromethane under rapid stirring below 0 °C aluminum. After continuing to stir for 1 hour, the resulting solution was slowly warmed to 10°C. A solution of 7.67 g (25.6 mmol) of 1,3-dibromoadamantane in dichloromethane (30 ml) was then slowly added dropwise. After stirring at this temperature for 3 hours the solution was poured into 30 ml of ice water. After acidification with concentrated hydrochloric acid, the organic phase was washed with sodium bicarbonate solution and water, dried with calcium chloride, and the solvent was removed. The crude product was isolated by distillation to give 3.2 g (75%) (B.p. 90-92° / 15 mmHg).
Embodiment 2
[0030] Add 1.1 mL (1.72 g, 11 mmol) of titanium tetrachloride and 0.13 g (1 mmol) of titanium trichloride to 100 mL of dimethylzinc (1M) in dichloromethane under rapid stirring below 0 °C aluminum. After continuing to stir for 1 hour, the resulting solution was slowly warmed to 5°C. A solution of 7.67 g (25.6 mmol) of 1,3-dibromoadamantane in dichloromethane (15 ml) was then slowly added dropwise. After stirring at this temperature for 3 hours the solution was poured into 30 ml of ice water. After acidification with concentrated hydrochloric acid, the organic phase was washed with sodium bicarbonate solution and water, dried with calcium chloride, and the solvent was removed. The crude product was isolated by rectification to obtain 3.5 g (82%) (B.p.90-92°C / 15mmHg).
Embodiment 3
[0032] To 100 ml of dimethylzinc (1M) in dichloromethane, 1.1 ml (1.72 g, 11 mmol) of titanium tetrachloride and 0.26 g (2 mmol) of trichloride were added below 0°C with rapid stirring. aluminum. After continuing to stir for 1 hour, the resulting solution was slowly warmed to 10°C. A solution of 7.67 g (25.6 mmol) of 1,3-dibromoadamantane in dichloromethane (15 ml) was then slowly added dropwise. After stirring at this temperature for 3 hours the solution was poured into 30 ml of ice water. After acidification with concentrated hydrochloric acid, the organic phase was washed with sodium bicarbonate solution and water, dried with calcium chloride, and the solvent was removed. The crude product was isolated by rectification to obtain 3.4 g (80%) (B.p.90-92° / 15 mmHg).
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