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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20305생성일: 2026년 10월 25일

Benzylamine → 1-(1,1-dimethylethyl)-N-(phenylmethyl)-4-Piperidinamine

https://huagongshe.com/reaction/20305

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물1-tert-Butyl-4-piperidoneHCID 73840—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Acetic AcidHCID 176—
생성물1-(1,1-dimethylethyl)-N-(phenylmethyl)-4-PiperidinamineHCID 2264793926.3%

반응 단계

A solution of 1-tert-butyl-4-oxopiperidine (3.6 g, 23.1), benzylamine (5.11 ml, 46.8 mmol), acetic acid (1.5 ml) and sodium triacetoxyborohydride (7.38 g, 34.8 mmol) was stirred at ambient for 2 days. Reaction mixture reduced in vacuo, residue partitioned between aqueous K2CO3 and EtOAc. The organic portion was dried (Na2SO4), filtered and reduced in vacuo. The residue was subjected to chromatography using CH2Cl2/MeOH/NH4OH (87/12/1) as the eluent to yield N-benzyl-1-tert-butylpiperidin-4-amine (1.5 g) (LC/MS: Rt 0.45, [M+H]+ 247).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745638B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-48e4777ee5c849119137dbc7f8327e03
출처 메모uspto-grants-2010_06