Reacción #487556
ord-7924f9c02d58491d97b9f855f93dc1bc
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONis added dropwise over 30 minutes
- 2workup.STIRRINGthe reaction mixture is stirred for two hours
- 3workup.ADDITIONonce the addition
- 4workup.STIRRINGis stirred for two hours
- 5ConcentraciónThe mixture is concentrated
- 6Otroto remove most of the tetrahydrofuran
- 7workup.ADDITIONdiluted with water
- 8Extracciónextracted with diethyl ether
- 9LavadoThe organic extracts are washed with water and brine
- 10Secadodried over anhydrous sodium sulfate
- 11Filtraciónfiltered
- 12Otrothe filtrate is evaporated in vacuo
- 13OtroThe residue is further purified by flash column chromatography on silica gel
- 14Lavadoeluting with 7% ethyl acetate in hexane
Procedimiento
3-Bromo-4′-chloro-4-ethylbiphenyl (10 g, 0.03 mol) is dissolved in tetrahydrofuran (250 ml), and the temperature is cooled to −78° C. n-Butyllithium (1.33 molar solution in hexanes, 34.6 ml) is added dropwise over 30 minutes, maintaining the temperature at around −78° C. The reaction mixture is stirred for one and a half hours, then trimethylborate (4.9 g, 0.05 mol) is added dropwise and the reaction mixture is stirred for two hours. A solution of 2N aqueous hydrochloric acid (100 ml) is added dropwise, and once the addition is complete the mixture is stirred for two hours. The mixture is concentrated to remove most of the tetrahydrofuran, then diluted with water and extracted with diethyl ether. The organic extracts are washed with water and brine, combined, dried over anhydrous sodium sulfate, filtered and the filtrate is evaporated in vacuo. The residue is further purified by flash column chromatography on silica gel, eluting with 7% ethyl acetate in hexane to give 4′-chloro-4-ethylbiphen-3-ylboronic acid (5.4 g).