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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1864915생성일: 2026년 10월 27일

1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate → 1-Benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1864915

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylateHCID 58893186—
반응물HCID 178418287HCID 178418287—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl 4-methyl 4-(2-oxoethyl)piperidine-1,4-dicarboxylateHCID 58893182—

반응 단계

To a solution of 1-benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate from Step B (4.45 g, 14.0 mmol) in THF (70 mL) at 0° C. was added borane-methyl sulfide complex (28.0 mL of a 2M solution in THF, 56.1 mmol). The reaction mixture was slowly warmed to ambient temperature and stirred for 16 h, then quenched with water and concentrated in vacuo. The residue was dissolved in CH2Cl2 (140 mL) and added drop wise to a solution of PCC (6.65 g. 30.8 mmol) and 4 Å molecular sieves (6.65 g) in CH2Cl2 (50 mL) at 0° C. The reaction mixture was warmed to ambient temperature and stirred for 16 h, then diluted with ether (200 mL) and filtered through a pad of celite. Additional ether was used to wash the celite. The combined organics were concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH-100:0 to 95:5, to give the title compound. MS: m/z=356 (M+Na).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625901B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-9495b06a2b7f47d689f4fb3ebd02d74b
출처 메모uspto-grants-2009_12