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HRID 267193作成日:2026年10月26日

Potassium borohydride → 4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanol

https://huagongshe.com/reaction/267193

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium borohydrideHCID 4192641—
反応物Sodium MethoxideHCID 10942334—
反応物4-[4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]piperidino]butyrophenone hydrochlorideHCID 21555731—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物4-[alpha-(p-Tert-butylphenyl)-alpha-hydroxybenzyl]-alpha-phenyl-1-piperidinebutanolHCID 21555715—

反応手順

To a mixture of 4.2 g (0.0083 mole) of 4-[4-[α-(p tert-butylphenyl)-α-hydroxybenzyl]piperidino]butyrophenone hydrochloride and 0.54 g (0.01 mole) of sodium methoxide in 25 ml of methanol is added 2.16 g (0.04 mole) of potassium borohydride. The reaction mixture is stirred overnight, diluted with water and the methanol removed under reduced pressure. The remaining material is extracted with chloroform, washed with water, dried over magnesium sulfate and filtered. The filtrate is concentrated, and the residue is recrystallized from acetone-water to give 4-[α-(p-tert-butylphenyl)-α-hydroxybenzyl]-α-phenyl-1-piperidinebutanol, M.P. 161°-163°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03941795
出典データセットuspto-grants-1976_03
ORD IDord-31d54994f1804563936e334fbdce7530
出典メモuspto-grants-1976_03