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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 650521생성일: 2026년 10월 24일

Sodium hydride → tert-Butyl 4-cyano-4-(2-methylphenyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/650521

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-(o-Tolyl)acetonitrileHCID 31155—
반응물N-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물tert-Butyl 4-cyano-4-(2-methylphenyl)piperidine-1-carboxylateHCID 22625983—

반응 단계

A solution of bis(2-chloroethyl)-N-(1,1-dimethylethoxy)carbonyl amine (1.438 g, 5.94 mmol) and 2-methylphenyl acetonitrile (600 mg, 3.96 mmol) in a 4:1 mixture of THF/DMF (15 mL) was treated with NaH (357.9 mg, 8.7 mmol) at 60° C. (3 d). The solvent was removed in vacuo, the residue dissolved in EtOAc (200 ml) and washed with saturated NaHCO3 (50 ml), H2O (2×50 ml), and saturated aqueous NaCl (50 ml), dried (Na2SO4) and concentrated in vacuo. PCTLC (SiO2, 6 mm, 100% hexane) afforded 4-cyano-N-(1,1-dimethylethoxy)carbonyl-4-(2-methylphenyl) piperidine as a yellow/orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06274583B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-47a2f0d30788418ca2bdd90ab93eaf59
출처 메모uspto-grants-2001_08