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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279301생성일: 2026년 10월 26일

Sodium Hydroxide → 1-(4-ethylbenzyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine

https://huagongshe.com/reaction/279301

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-EthylbenzaldehydeHCID 20861—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidineHCID 54359471—
용매DichloromethaneHCID 6344—
용매Acetic acid methanolHCID 10129899—
생성물1-(4-ethylbenzyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidineHCID 6921453662.1%

반응 조건

온도60 °C

반응 단계

To A solution of 4-[{N-(9-fluorenylmethyloxycarbonyl)glycyl}aminomethyl]piperidine (1.00 g, 2.33 mmol) in 2.5% AcOH/CH3OH (80 mL) were added 4-ethylbenzaldehyde (1.09 g, 8.16 mmol) and NaBH3CN (6.59 g, 10.5 mmol). The reaction mixture was stirred at 60° C. for 13 h. After the mixture was cooled to room temperature, 1 N aqueous NaOH solution (50 mL) and dichloromethane (50 mL) were added. The organic layer was separated and the aqueous layer was extracted with dichloromethane (50 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Column chromatography (SiO2, CH3OH/AcOEt 2:8) afforded 1-(4-ethylbenzyl)-4-[{N-(9-fluorenylmethyloxycarbonyl)glycyl}aminomethyl]piperidine (740 mg, 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-28816753564344f381a3a137ea241819
출처 메모uspto-grants-2002_03