Molecular Formula | C6H6BClO3 |
Molar Mass | 172.37 |
Density | 1.49±0.1 g/cm3(Predicted) |
Melting Point | 166-170 |
Boling Point | 369.3±52.0 °C(Predicted) |
Flash Point | 177.131°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 7.63±0.58(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Refractive Index | 1.602 |
Hazard Symbols | Xi - Irritant![]() |
Risk Codes | 41 - Risk of serious damage to eyes |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S39 - Wear eye / face protection. |
Hazard Note | Irritant |
Introduction | 5-chloro-2-hydroxyphenylboronic acid is an organic intermediate, it is reported in the literature that it can be obtained by using 5-chloro-2-methoxyphenyl boronic acid as a raw material and removing methyl. |
preparation | 5-chloro-2-methoxyphenylboronic acid (10.0g,53.6mmol) in dichloromethane (100ml) the solution was cooled to a temperature of 5-10 °c. 100ml of 1m boron tribromide solution in DCM was added dropwise to the above mixture over a period of 30 minutes using a pressure-equalizing dropping funnel. The resulting reaction mixture was then stirred at room temperature for 30 minutes. After completion of the reaction, the mixture was poured Dropwise into ice-cold saturated sodium bicarbonate solution (600ml). The resulting mixture was allowed to stir at room temperature for 1 hour. The DCM layer was separated and the aqueous layer thus collected was cooled to a temperature of 10-15 °c. A 1N dilute hydrochloric acid solution was then added to the cooled aqueous layer as described above, and this resulted in the formation of a precipitate. The solid was filtered off under vacuum and dried to afford 9G (97% yield) of product. |