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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772582Generated: November 2, 2026

Chlorotrimethylsilane → HCID 86731802, compound

https://huagongshe.com/reaction/1772582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantTrimethoxysilaneHCID 17215—
Reactant2-(prop-2-en-1-yloxy)ethanamineHCID 261273—
CatalystPlatinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxaneHCID 10959889—
SolventTolueneHCID 1140—
ProductHCID 86731802HCID 8673180286%

Reaction Steps

After adding toluene (200 mL) to a round-bottom flask containing 2-(allyloxy)ethanamine (0.398 mol) and dissolving trimethoxysilane (0.398 mol), a commercially available platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane solution was added and the mixture was stirred for 24 hours. Upon completion of reaction, after removing the solvent through distillation under reduced pressure and extracting with water and diethyl ether, the product was dissolved in dichloromethane (200 mL). After adding triethylamine (1.0 mol) and trimethylchlorosilane (0.8 mol), the mixture was stirred for a day at room temperature. Upon completion of reaction, after removing the solvent through distillation under reduced pressure, 0.342 mol (yield: 86%) of the target compound was obtained by extracting with water and diethyl ether. 1H and 13C NMR spectroscopic data of the purified N,N-bis(trimethylsilyl)-2-(3-(trimethoxysilyl)propoxy)ethanamine are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249276B2
Source datasetuspto-grants-2016_02
ORD IDord-f9137ce9facd44a19be7f5f6e1dc9e49
Source noteuspto-grants-2016_02