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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046299생성일: 2026년 10월 26일

Acetic Acid → 1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/1046299

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Methyl 4-FormylbenzoateHCID 15294—
반응물tert-Butyl 2-(aminomethyl)piperidine-1-carboxylateHCID 2756482—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매1,1-DichloroethaneHCID 6365—
생성물1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylateHCID 6848915796.6%

반응 단계

A solution of 1-Boc-2-aminomethylpiperidine (429 mg, 2 mmol) and methyl 4-formylbenzoate (329 mg, 2 mmol) in dichloroethane (10 mL) was stirred as acetic acid (180 mg, 3 mmol) and sodium triacetoxyborohydride (487 mg, 2.3 mmol) were added sequentially. The reaction was stirred at ambient temperature for 17 hours. The reaction was poured into water and extracted with methylene chloride (2×). The organic phase was dried over sodium sulfate, filtered, and concentrated. Purification on silica gel using a gradient of ethyl acetate in hexane gave 0.7 g of 1,1-dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569303B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-a4af34579fff4ba78e1753f5c4d0274e
출처 메모uspto-grants-2013_10