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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1510590생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1510590

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methacryloyl chlorideHCID 13528—
반응물AminopropyltrimethoxysilaneHCID 83756—
촉매Phenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
용매DichloromethaneHCID 6344—
생성물2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-HCID 1387916771.6%

반응 단계

77.4 g 3-(amino)propyltrimethoxysilane, 43.7 g triethylamine and 25 mg di-tert-butyl-p-cresol were dissolved in 500 ml dichloromethane under argon. 45.1 g methacryloyl chloride was slowly added dropwise within 1 h at −5° C., after which stirring was continued for a further 1 h at 0° C. The precipitated hydrochloride was filtered off and washed again with dichloromethane. The volatile components were removed at 40° C. under reduced pressure on the rotary evaporator. A yellow liquid with separated 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 to small volume by introducing dry air at 40° C. on the rotary evaporator. The brownish liquid was freed from the remaining volatile components at 4 Pa (4×10−2 mbar) and the crude product (104.2 g) was distilled at a pressure of 0.06 Pa (6×10−4 mbar). The product had a boiling point of 123-125° C. 76.4 g product was obtained as a yellowish clear liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08211956B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-16dca3105f45499c8abffe43ddda2c9a
출처 메모uspto-grants-2012_07