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HRID 1637301作成日:2026年10月27日

2,4-Dimethyl-6-tert-butylphenol → 4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoate

https://huagongshe.com/reaction/1637301

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dimethyl-6-tert-butylphenolHCID 15884—
反応物4-(4-Bromobutoxy)phenyl 4-allyloxybenzoateHCID 19348983—
反応物Potassium methacrylateHCID 23667354—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒tert-Butyl methyl etherHCID 15413—
生成物4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoateHCID 2199961883%

反応条件

温度100 °C

反応手順

118.4 g (0.29 mol) of this ester were dissolved in 50 ml of dimethylformamide at 70° C., 0.3 g of 2-tert-butyl-4,6-dimethylphenol was added as stabilizer, 111.7 g (0.9 mol) of dry potassium methacrylate salt were added, and the mixture was diluted with 70 ml of toluene. The reaction mixture was stirred at 100° C. for 6 h, then cooled and diluted with 800 ml of methyl tert-butyl ether. The precipitate was filtered off with suction, and the washing solution and the filtrate were combined and washed three times with water. They were then concentrated, and the crude product obtained was recrystallized from isopropanol. 4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoate of m.p. 62-63° C. was obtained in a yield of 83%. Between 41 and 45° C. the ester has a nematic phase which occurs only on supercooling.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06040411
出典データセットuspto-grants-2000_03
ORD IDord-f2119b27a66f42e48695240ef4e4ba8d
出典メモuspto-grants-2000_03