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HRID 258955作成日:2026年10月26日

N,N-Dimethylbenzylamine → HCID 21425139、化合物

https://huagongshe.com/reaction/258955

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylbenzylamineHCID 7681—
反応物TrichloropentylsilaneHCID 7885—
反応物alpha-BromoethyltriethoxysilaneHCID 21425138—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物HCID 21425139HCID 21425139—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04035411
出典データセットuspto-grants-1977_07
ORD IDord-c4e838e1b7d3491287275096ae3d8e91
出典メモuspto-grants-1977_07