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HRID 1638373作成日:2026年10月25日

Water → 3-(4-Chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanol

https://huagongshe.com/reaction/1638373

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-[2-(4-Chlorophenoxy)propan-2-yl]-2-(4-chlorophenyl)oxiraneHCID 19842485—
反応物HCID 178507082HCID 178507082—
溶媒1-PropanolHCID 1031—
生成物3-(4-Chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanolHCID 1321740918.4%

反応手順

A solution of 30 g (0.093 mol) of 2-(4-chlorophenyl)-2-[2-(p-chlorophenoxy)-prop-2-yl]-oxirane in 40 ml of n-propanol is added dropwise to a solution of 7.6 g (0.107 mol) of 1,2,4-triazolyl-sodium in 60 ml of n-propanol, at room temperature. The reaction mixture is stirred at the reflux temperature for a further 48 hours and is cooled, water is added and the mixture is extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated in vacuo. The oily residue is purified by column chromatography. 6.7 g (18.4% of theory) of 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-butan-2-ol are obtained. This is stirred with 20 ml of saturated hydrogen chloride/ether solution, at room temperature. The precipitate which separates out is filtered off under suction, rinsed with a small amount of ether and dried in vacuo at 40° C. 6.5 g (89% of theory, relative to base employed) of 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-butan-2-ol hydrochloride of melting point 135° C. are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04879385
出典データセットuspto-grants-1989_11
ORD IDord-8484bafb02124fc191289652a083bf76
出典メモuspto-grants-1989_11