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HRID 384570作成日:2026年10月26日

Triethylamine → 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-

https://huagongshe.com/reaction/384570

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methacryloyl chlorideHCID 13528—
反応物AminopropyltrimethoxysilaneHCID 83756—
触媒Phenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
溶媒DichloromethaneHCID 6344—
生成物2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-HCID 1387916771.6%

反応条件

温度0 °C

反応手順

77.4 g 3-(amino)propyltrimethoxysilane, 43.7 g triethylamine and 25 mg di-tert.-butyl-p-cresol were dissolved under argon in 500 ml dichloromethane. 45.1 g methacryloyl chloride was slowly added dropwise at −5° C. within 1 h, and the whole was then stirred for 1 h at 0° C. The precipitated hydrochloride was filtered off and washed with dichloromethane. The volatile constituents were removed at 40° C. under reduced pressure using the rotary evaporator. A yellow liquid with precipitated solid (hydrochloride) remained. The precipitation of the hydrochloride was completed by adding 150 ml diethyl ether, the precipitate was filtered off and the filtrate concentrated at 40° C. using a rotary evaporator with introduction of dry air. The brownish liquid was freed of residual volatile constituents at 4×10−2 mbar, and the raw product (104.2 g) was distilled at a pressure of 6×10−4 mbar. The product had a boiling point of 123-125° C. 76.4 g of product was obtained as yellowish, clear liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367748B2
出典データセットuspto-grants-2013_02
ORD IDord-fba6205435e44ca9aa904b779077e896
出典メモuspto-grants-2013_02