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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16490생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/16490

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 번호US07737145B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1c2642caec064d1e85d8d4390dbe9730
출처 메모uspto-grants-2010_06