HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384570Generated: October 25, 2026
Triethylamine → 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-
https://huagongshe.com/reaction/384570
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Aminopropyltrimethoxysilane | HCID 83756 | — |
| Catalyst | Phenol, bis(1,1-dimethylethyl)-4-methyl- | HCID 3034427 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]- | HCID 13879167 | 71.6% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367748B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-fba6205435e44ca9aa904b779077e896 |
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| Source note | uspto-grants-2013_02 |
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