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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058779생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1058779

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ChlorideHCID 5234—
반응물1,4-DifluorobenzeneHCID 10892—
반응물Sodium hydrideHCID 24758—
반응물Phenyl-piperidin-4-yl-methanolHCID 339086—
반응물Potassium BenzoateHCID 23661960—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidineHCID 1866935854%

반응 조건

온도72.5 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518284B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-49fa5571b1d440ebad6f0f55ec530ec2
출처 메모uspto-grants-2003_02