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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373208Generated: October 30, 2026

Water → N-(3-(1,1,1,5,5,5-Hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propyl)methacrylamide

https://huagongshe.com/reaction/373208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantMethacryloyl chlorideHCID 13528—
Reactant(3-Aminopropyl)tris(trimethylsiloxy)silaneHCID 2756547—
SolventDiethyl EtherHCID 3283—
ProductN-(3-(1,1,1,5,5,5-Hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propyl)methacrylamideHCID 16051444—

Reaction Steps

In 200 ml of ethyl ether was dissolved 36.6 g of the 3-[tris(trimethylsiloxy)silyl]propylamine obtained above, and the solution was added with 9.5 g of pyridine. The mixture was cooled in ice bath to 0°-5° C. Separately, 12.6 g of methacryloyl chloride was dissolved in 30 ml of ethyl ether. The methacryloyl chloride solution was placed in a separating funnel and dropped therefrom to the above mixture over about one hour. The mixture was continuously stirred for 16 hours. After the stirring, 200 ml of water was added to the reaction mixture, and the resulting mixture was stirred and the supernatant was separated. The supernatant was combined with the extract from the bottom layer with ethyl ether, and then ethyl ether was removed by heating. The residue was distilled in vacuo to give 36.6 g of a distillate at 165° C./2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162391
Source datasetuspto-grants-1992_11
ORD IDord-1b0edaf3d91c4a48b9db9f0155376c58
Source noteuspto-grants-1992_11