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HRID 432544作成日:2026年10月27日

Imidazole → tert-Butyl(dimethyl)[(6-phenylhexyl)oxy]silane

https://huagongshe.com/reaction/432544

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Sodium BicarbonateHCID 516892—
反応物6-Phenyl-1-hexanolHCID 520110—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl(dimethyl)[(6-phenylhexyl)oxy]silaneHCID 69823535—

反応手順

The procedure used was similar to that described by Corey and Venkateswarlu (Corey, E. J.; Venkateswarlu, A., J. Am. Chem. Soc., 1972, 94, 6190-6191). 6-Phenyl-1-hexanol (14.0 g) and imidazole (13.36 g) were dissolved in dry DMF (40 mL). tert-Butyldimethylsilyl chloride (14.20 g,) was then added in one portion. The resulting solution was allowed to stir for 8 hours at room temperature. Aqueous sodium bicarbonate (100 mL, 10% by wt.) was then added and the resulting solution was allowed to stir for 15 minutes. The desired product was then extracted from the mixture with petroleum ether (3×250 mL). The petroleum ether extract was then washed with distilled H2O (7×300 mL), dried over MgSO4 and roto-evaporated to give the desired product as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664111B2
出典データセットuspto-grants-2003_12
ORD IDord-a1316664cb9d4486913a01ec8d7167c7
出典メモuspto-grants-2003_12