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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1712305생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1712305

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,3,2-Dioxathiolane, 2,2-dioxideHCID 14075—
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl 3-hydroxy-4-(4-methoxyphenyl)piperidine-1-carboxylateHCID 45074240—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 3-(2-hydroxyethoxy)-4-(4-methoxyphenyl)piperidine-1-carboxylateHCID 68501804—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790715B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-2f9ad858c81241e88ad54b00f68ea783
출처 메모uspto-grants-2010_09