関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methacryloyl chloride | HCID 13528 | — |
| 反応物 | Aminopropyltrimethoxysilane | HCID 83756 | — |
| 触媒 | Phenol, bis(1,1-dimethylethyl)-4-methyl- | HCID 3034427 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]- | HCID 13879167 | 71.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08367748B2 |
|---|
| 出典データセット | uspto-grants-2013_02 |
|---|
| ORD ID | ord-fba6205435e44ca9aa904b779077e896 |
|---|
| 出典メモ | uspto-grants-2013_02 |
|---|