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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258955Generated: October 25, 2026

N,N-Dimethylbenzylamine → HCID 21425139, compound

https://huagongshe.com/reaction/258955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylbenzylamineHCID 7681—
ReactantTrichloropentylsilaneHCID 7885—
Reactantalpha-BromoethyltriethoxysilaneHCID 21425138—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 21425139HCID 21425139—

Reaction Steps

In a manner like that used for the preparation of alpha-bromoethyltriethoxysilane, alpha-bromoamyltriethoxysilane is prepared in two steps from amyltrichlorosilane (commercially available). One-quarter mole of alpha-bromoamyltriethoxysilane (78.5g) is refluxed for 12 hours with 0.25 moles (33.75g) of benzyldimethylamine in 125 ml. of 2-butanone. The product, alpha-(benzyldimethylammonio)ethyltriethoxysilane bromide is isolated by removing the solvent under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035411
Source datasetuspto-grants-1977_07
ORD IDord-c4e838e1b7d3491287275096ae3d8e91
Source noteuspto-grants-1977_07