反応 #2195506
ord-3492063a70aa4749b51545e760e75ef3
反応方程式
反応条件
後処理
- 1その他equipped with a thermoregulator, stirrer
- 2温度cooling condenser
- 3workup.ADDITIONwas added dropwise at 75° C. to the obtained solution over 20 minutes
- 4その他After the obtained reaction mixture
- 5温度was cooled to room temperature
- 6workup.ADDITIONwas added
- 7洗浄the organic layer was then washed three times with 300 g of distilled water
- 8その他After methyl ethyl ketone was removed under reduced pressure
- 9その他the reaction product was precipitated in 300 ml of methanol
- 10その他to collect solid matter
- 11ろ過through filtration, which
- 12その他was then dried at 50° C. in a vacuum oven
実験手順
45 g (0.25 equivalent) of dicyclopentadiene skeleton phenolic resin, DPP-3H (special phenolic resin manufactured by Nippon Petrochemical Co., Ltd.), 38.1 g of vinylbenzyl chloride CMS-AM (m-/p-isomers: 50/50 wt % mixture) (purity of 91%, 0.25 mol), 2.4 g of tetra-n-butylammonium bromide, 0.038 g of 2,4-dinitrophenol and 200 g of methyl ethyl ketone were charged into a 1-liter four-necked flask equipped with a thermoregulator, stirrer, cooling condenser and dropping funnel and dissolved under agitation, and 40 g of a 50 wt % aqueous solution of NaOH (NaOH purity of 95%, 0.475 mol) was added dropwise at 75° C. to the obtained solution over 20 minutes and further stirred at 75° C. for 4 hours. After the obtained reaction mixture was cooled to room temperature, it was neutralized with 2N hydrochloric acid, 100 g of toluene was added, and the organic layer was then washed three times with 300 g of distilled water. After methyl ethyl ketone was removed under reduced pressure, the reaction product was precipitated in 300 ml of methanol to collect solid matter through filtration, which was then dried at 50° C. in a vacuum oven to obtain a vinylbenzyl ether compound at a yield of 95%. This is designated as compound 3.