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HRID 1058779作成日:2026年10月27日

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

https://huagongshe.com/reaction/1058779

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 1866935854%

反応条件

温度72.5 °C

反応手順

The alcohol prepared above (2.7 g, 9.3 mmol) dissolved in DMSO (25 mL) was added over an NaH (60%, 0.6 g) suspension in DMSO (5 mL). Potassium benzoate (1.53 g, 9.63 mmol) and 1,4-difluorobenzene (1.3 mL, 11.9 mmol) were added and the mixture was 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 (40 mL) and an aqueous hydrochloric acid (40 mL) solution for 1 h. Isolation of the product using the customary methodology provided (+)-4-[(4-fluorophenoxy)phenyl]methyl-piperidine as an oil in a 54% yield. Treatment of 0.5 g (1.75 mmol) of this oil with D-dibenzoyltartaric acid in ethanol (96%, 30 mL) provided a precipitate which was filtered (m.p.=198-199° C.). The aminoether was released yielding a white solid with a 96% ee, m.p.=102-104° C., and [α]546+15, c=0.105, 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-49fa5571b1d440ebad6f0f55ec530ec2
出典メモuspto-grants-2003_02