戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1176227作成日:2026年10月27日

Benzyl formate → Benzyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1176227

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl formateHCID 7708—
反応物Sodium CarbonateHCID 10340—
反応物4-{4-[3-(2-Methoxybenzyloxy)propoxy]phenyl}piperidin-3-olHCID 68503440—
溶媒Ethyl AcetateHCID 8857—
生成物Benzyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68499596—

反応手順

The solution of 3.0 g of 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidin-3-ol in 30 ml of ethyl acetate is cooled to 0° C. with stirring and admixed with 30 ml of saturated aqueous sodium carbonate solution. At 0-5° C., 1.32 ml of benzyl formate are added dropwise. After 10 minutes, the reaction mixture is poured onto water (250 ml) and extracted with ethyl acetate (2×250 ml). The organic phases are washed with brine (1×250 ml), 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=0.35 (1:1 EtOAc-heptane); Rt=5.94. m.p. 71-73° C.

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-ed19945ce2944ad89c9b8528d6d1a000
出典メモuspto-grants-2010_11