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HRID 1058781作成日:2026年10月25日

Hydrochloric Acid → (+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidine

https://huagongshe.com/reaction/1058781

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium ChlorideHCID 5234—
反応物1,4-DifluorobenzeneHCID 10892—
反応物Sodium hydrideHCID 24758—
反応物Phenyl-piperidin-4-yl-methanolHCID 339086—
反応物Potassium BenzoateHCID 23661960—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物(+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidineHCID 1866935864%

反応条件

温度72.5 °C

反応手順

The alcohol prepared above (1.3 g, 4.5 mmol) dissolved in DMSO (10 mL) was added over an NaH (60%, 210 g) suspension in DMSO (5 mL). Potassium benzoate (715 g, 4.5 mmol) and 1,4-difluorobenzene (0.75 mL, 6.86 mmol) were added and the mixture heated (70-75° C.) until the starting substance disappeared. The reaction mixture was poured into water and saturated aqueous NaCl solution, and extracted with ether. The oil obtained was refluxed with a mixture of methanol (17 mL) and an aqueous hydrochloric acid (17 mL) solution for 1 h. The usual working of the reaction provided (−)-4-[(4-fluorophenoxy)phenyl]methyl-piperidine as an oil in a 64% yield. Treatment of this oil with L-dibenzoyltartaric acid in ethanol (96%, 35 mL) provided a precipitate which was filtered (m.p.=193-194° C.). The aminoether was released yielding a white solid with a 98% ee, m.p.=100-102° C., and [α]546−14, c=0.2, CHCl3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06518284B2
出典データセットuspto-grants-2003_02
ORD IDord-bf4a815c6602482ab51787f9371fd8ff
出典メモuspto-grants-2003_02