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HRID 1176275作成日:2026年10月27日

Water → Tert-butyl 3-(2-hydroxyethoxy)-4-(4-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1176275

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,3,2-Dioxathiolane, 2,2-dioxideHCID 14075—
反応物Sodium hydrideHCID 24758—
反応物Tert-butyl 3-hydroxy-4-(4-methoxyphenyl)piperidine-1-carboxylateHCID 45074240—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 3-(2-hydroxyethoxy)-4-(4-methoxyphenyl)piperidine-1-carboxylateHCID 68501804—

反応手順

A solution of 1.01 g of tert-butyl 3-hydroxy-4-(4-methoxyphenyl)piperidine-1-carboxylate in 40 ml of N,N-dimethylformamide is added at 0° C. to the suspension of 0.26 g of sodium hydride dispersion (60%) in 40 ml of N,N-dimethylformamide. After 30 minutes, the reaction mixture is admixed with 0.83 g of [1,3,2]dioxathiolane 2,2-dioxide and stirred at room temperature over 18 hours. The reaction mixture is cooled to 0° C., admixed with water and concentrated by evaporation. The residue is stirred in a 1:10 mixture of 0.1 M H2SO4/dioxane at 50° C. over 60 hours, neutralized with saturated aqueous sodium hydrogencarbonate solution and concentrated by evaporation. The residue is dissolved in ethyl acetate, washed with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.20 (1:1 EtOAc-heptane); Rt=4.24.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07842688B2
出典データセットuspto-grants-2010_11
ORD IDord-bf0ed10be5b14d4ba022f8272fe8eab4
出典メモuspto-grants-2010_11