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HRID 1065633作成日:2026年10月25日

Triethylamine → 1-p-Phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butane

https://huagongshe.com/reaction/1065633

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物ChlorotriethylsilaneHCID 13819—
反応物BitertanolHCID 91656—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物1-p-Phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butaneHCID 2053955740.7%

反応条件

温度45 °C

反応手順

5.5 g of 1-p-phenylphenoxy-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol is dissolved in 25 ml of THF. 2.9 g of triethylchlorosilane and 0.2 g of 4-dimethylaminopyridine are added under a nitrogen blanket. The mixture is heated to 45° C., and 3.3 g of triethylamine is added in portions. After the mixture has been stirred for 14 hours at from 40° to 50° C. it is cooled to room temperature, undissolved matter is filtered off, and the filtrate is concentrated. The product is further purified either by adding petroleum ether, followed by filtration and concentration, or by gel filtration (SiO2, CHCl3). There is obtained 3 g of 1-p-phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04330535
出典データセットuspto-grants-1982_05
ORD IDord-2f9a22956e5947f0a32bdb954971dfd7
出典メモuspto-grants-1982_05