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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
ReactantAminopropyltrimethoxysilaneHCID 83756—
CatalystPhenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
SolventDichloromethaneHCID 6344—
Product2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-HCID 1387916771.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367748B2
Source datasetuspto-grants-2013_02
ORD IDord-fba6205435e44ca9aa904b779077e896
Source noteuspto-grants-2013_02