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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2239528생성일: 2026년 10월 26일

Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate → 1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazine

https://huagongshe.com/reaction/2239528

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylateHCID 58812409—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazineHCID 5829982488%

반응 단계

A mixture of benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate (Method 90, 2.1 g, 5.55 mmol) and Pd/C (0.059 g, 0.55 mmol) in methanol (30 mL) was stirred under H2 (g) for 24 hours. The reaction mixture was filtered through a pad of Celite and concentrated under reduced pressure to give 1.20 g, (88%) of a yellow oil. 1H NMR: CD3Cl 3.74 (t, 2H), 2.90 (m, 4H), 2.51 (m, 6H), 0.88 (s, 9H), 0.04 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07723337B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-598620f990ba4d77a236db01de1f2e4d
출처 메모uspto-grants-2010_05