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HRID 1383079作成日:2026年10月27日

Water → Triapenthenol

https://huagongshe.com/reaction/1383079

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium metaborateHCID 145326—
反応物1-Cyclohexyl-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-oneHCID 56609707—
溶媒TetrahydrofuranHCID 8028—
生成物TriapenthenolHCID 6437842—

反応手順

0.68 g (0.018 mol) of sodium boranate is added to a suspension of 5.2 g (0.018 mol) of S-2-(dibenzyl-hydroxymethyl)-pyrrolidine hydrochloride in 75 ml of absolute tetrahydrofuran at -30° C., with stirring. The temperature is allowed to rise gradually to 20° C. and stirring is continued at 20° C. for a further 2 hours. Thereafter, 3.15 g (0.012 mol) of the (E)-isomer of 1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pent-1-en-3-one are added dropwise and the mixture is stirred at 40° C. for 20 hours. The reaction mixture is then poured into water. The resulting mixture is extracted with ethyl acetate and the combined organic phases are concentrated uner reduced pressure. The residue which remains is chromatographed with a mixture of chloroform/ethyl acetate=4:1 on silica gel. 2.1 g (67% of theory) of the (-)-antipode of (E)-1-cyclohexyl-4,4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene are obtained on this manner in the form of a crystalline product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04808725
出典データセットuspto-grants-1989_02
ORD IDord-6c1ba379364c49cbbd8f87cbc1c49e43
出典メモuspto-grants-1989_02