참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methacryloyl chloride | HCID 13528 | — |
| 반응물 | Aminopropyltrimethoxysilane | HCID 83756 | — |
| 촉매 | Phenol, bis(1,1-dimethylethyl)-4-methyl- | HCID 3034427 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]- | HCID 13879167 | 71.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08211956B2 |
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| 출처 데이터셋 | uspto-grants-2012_07 |
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| ORD ID | ord-16dca3105f45499c8abffe43ddda2c9a |
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| 출처 메모 | uspto-grants-2012_07 |
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