Reacción #53765
ord-4896137c19754718b0fb141a71c5dfc7
Ecuación de reacción
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroequipped with a stirrer
- 2workup.ADDITIONto mix
- 3Filtraciónwas filtered
- 4Otrothus 365 g of a crude product was obtained
- 5Lavadowas subsequently washed with water
- 6OtroThe resulting organic liquid was dried
- 7FiltraciónAfter filtration
- 8Concentraciónthe liquid was concentrated
- 9Otroto stand at 0° C., so that a yellow solid
- 10Otrowas precipitated
- 11FiltraciónThe precipitate was filtered
- 12Lavadosubsequently washed with toluene
- 13Otroby drying
Procedimiento
In a three-liter flask having four openings equipped with a stirrer, a thermometer, a dropping funnel, and a reflux condenser, respectively, 256 g (1.4 mol) of fluorenone, 1 L of water, three drops of a surfactant, and five drops of sulfuric acid were placed and stirred to mix. By adding 250 g (1.6 mol) of bromine into the mixture, a reaction was started. After the reaction had been conducted at 50° C. for 12 hours, unreacted bromine was decomposed with an aqueous solution of sodium hydrogen sulfite. The reaction product, which was a dark yellow solid, was filtered and thus 365 g of a crude product was obtained. The crude product was dissolved in toluene and was subsequently washed with water and a sodium hydrogencarbonate aqueous solution. The resulting organic liquid was dried using anhydrous magnesium sulfate. After filtration, the liquid was concentrated and then allowed to stand at 0° C., so that a yellow solid was precipitated. The precipitate was filtered and subsequently washed with toluene, followed by drying. Thus, 339 g (1.3 mol, yield of 92%) of a yellow solid product was obtained. This product was subjected to gas chromatography and the purity of the product was 99.4%.