反应详情

温度

50 °C

A reaction was carried out by (a) feeding 23 g of fluorenone, 1.3 g of dodecyl mercaptan, and 161.0 g of 2-methyl phenol into a 500 ml glass reactor vessel equipped with a stirrer, a condenser and a thermometer, (b) dropping 13.0 g of 35% hydrochloric acid to a mixture, and (c) stirring the mixture at 50° C. for 2 hours. The amount of remaining fluorenone was determined by HPLC, and found to be 0.1% or less. To an obtained reaction mixture liquid, 18.5 g of 29% sodium hydroxide aqueous solution was added, and thereafter 94.0 g of 2-methyl phenol was distilled away from an organic phase by concentration under reduced pressure. To an obtained concentrated liquid, 161 g of toluene and 23 g of water were added, and the mixture liquid was stirred at 80° C. Thereafter, an aqueous phase was separated and removed, and a target substance partitioned in the organic phase was recovered. The organic phase was further washed twice with 23 g of water, and cooled to 10° C. Then, precipitated crystals were subjected to filtration and drying to obtain 37.9 g of 9,9-bis(4-hydroxy-3-methylphenyl)fluorene (yield: 84.3%, LC purity: 99.3%). Obtained 9,9-bis(4-hydroxy-3-methylphenyl)fluorene was dissolved by heat at 230° C. for 2 hours. The 9,9-bis(4-hydroxy-3-methylphenyl)fluorene thus dissolved had a hue of 1 in Gardner. The total amount of toluene used in the production was 4.2 parts by weight relative to 1 part by weight of the 9,9-bis(4-hydroxy-3-methylphenyl)fluorene.

1. customequipped with a stirrer, a condenser
2. additionwas added
3. distillation94.0 g of 2-methyl phenol was distilled away from an organic phase by concentration under reduced pressure
4. concentrationTo an obtained concentrated liquid, 161 g of toluene and 23 g of water
5. additionwere added
6. stirringthe mixture liquid was stirred at 80° C
7. customThereafter, an aqueous phase was separated
8. customremoved
9. customa target substance partitioned in the organic phase
10. customwas recovered
11. washThe organic phase was further washed twice with 23 g of water
12. temperaturecooled to 10° C
13. customThen, precipitated crystals
14. filtrationwere subjected to filtration
15. customdrying