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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61464생성일: 2026년 10월 24일

tert-Butyl bromoacetate → Dimethyl (2s,3s,5s)-5-(2-tert-butoxy-2-oxoethoxy)-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-1,3-dicarboxylate

https://huagongshe.com/ko/reaction/61464

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl bromoacetateHCID 79177—
반응물Potassium tert-butoxideHCID 23665647—
반응물dimethyl(2S,3S,5S)-5-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-1,3-dicarboxylateHCID 67304346—
용매TetrahydrofuranHCID 8028—
생성물Dimethyl (2s,3s,5s)-5-(2-tert-butoxy-2-oxoethoxy)-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-1,3-dicarboxylateHCID 67303979—

반응 단계

To a solution of dimethyl(2S,3S,5S)-5-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-1,3-dicarboxylate (50.0 mg, 0.000123 mol) in tetrahydrofuran (0.50 mL, 0.0062 mol) was added 1.00 M of potassium tert-butoxide in tetrahydrofuran (0.150 mL). After stirred at rt for 30 min, to the mixture was added bromo-acetic acid 1,1-dimethylethyl ester (0.0228 mL, 0.000154 mol). The resulting mixture was stirred at rt overnight and then concentrated to dry.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440958B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-49b234f9b422415a9b2b2e56258cad61
출처 메모uspto-grants-2016_09