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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132200생성일: 2026년 10월 25일

Tert-butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate → tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/132200

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 10377658—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylateHCID 151428097%

반응 단계

tert-Butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate (35.71 g, 140 mmol) was dissolved in a mixture of ethyl acetate (110 mL) and methanol (110 mL). 50% wet 10% palladium on carbon (3.3 g) was added to the mixture. Reaction vessel was charged with 55 psi of hydrogen gas. Reaction shook on a Parr apparatus at room temperature for 16 hours. Reaction mixture was filtered to remove the catalyst. Filtrate was concentrated in vacuo. Title compound was obtained as clear colorless oil in 97% yield. 1H NMR (300 MHz, CDCl3): δ=4.04 (d, J=10.25, 2H), 3.64 (s, 3H), 2.68 (t, J=12.44, 2H), 2.21 (d, J=6.95, 2H), 1.98-1.77 (m, 1H), 1.64 (d, J=13.54, 2H), 1.41 (s, 9H), 1.25-0.99 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384930B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-147cf76ce6814cbcbb42449da14866f2
출처 메모uspto-grants-2008_06