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HRID 547183作成日:2026年10月26日

Water → (R)-(1-methylpiperidin-3-yl)methanol

https://huagongshe.com/reaction/547183

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 HydroxideHCID 14798—
反応物ethyl (3R)-1-methylpiperidine-3-carboxylateHCID 736036—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-(1-methylpiperidin-3-yl)methanolHCID 92011394.3%

反応条件

温度20 °C

反応手順

A solution of (R)-ethyl 1-methylpiperidine-3-carboxylate (5.69 g, 33 mmol) in ether (20 ml) was added dropwise to a stirred solution of lithium aluminum hydride (36.6 ml of a 1M solution in THF, 36.6 mmol) in ether (85 ml) cooled to maintain a reaction temperature of 20° C. The mixture was stirred for 1.5 hours at ambient temperature and then water (1.4 ml), 15% aqueous sodium hydroxide solution (1.4 ml) and then water (4.3 ml) were added. The insolubles were removed by filtration and the volatiles removed from the filtrate by evaporation to give (R)-(1-methylpiperidin-3-yl)methanol (4.02 g, 94%) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE042353E1
出典データセットuspto-grants-2011_05
ORD IDord-358144f660614c7e80a93663495202a3
出典メモuspto-grants-2011_05