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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-Ethylbenzaldehyde | HCID 20861 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | 4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine | HCID 54359471 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Acetic acid methanol | HCID 10129899 | — |
| 생성물 | 1-(4-ethylbenzyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine | HCID 69214536 | 62.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06362177B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-28816753564344f381a3a137ea241819 |
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| 출처 메모 | uspto-grants-2002_03 |
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