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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1529542생성일: 2026년 10월 27일

Hydrogen Bromide → Ethyl 3-bromo-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1529542

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물BromineHCID 24408—
반응물Ethyl 4-oxo-1-piperidinecarboxylateHCID 34767—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-bromo-4-oxopiperidine-1-carboxylateHCID 13799628108%

반응 단계

Bromine (2.83 mL, 55 mmol) was added dropwise to a stirred solution of N-carbethoxy-4-piperidone (7.54 mL, 50 mmol) and a 48% solution of HBr in H2O (1.41 mL) in THF (88 mL) at 0° C. The mixture was stirred at room temperature for 15 minutes and then quenched with a saturated solution of Na2S2O3, basified with a saturated solution of Na2CO3 and extracted with diethyl ether. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo to yield 3-bromo-4-oxo-1-piperidinecarboxylic acid ethyl ester (13.5 g, 54% yield, 50% pure) as a dark brown oil that was used in the next step without further purification. C8H12BrNO3 GCMS (EI): Rt 3.77, MW (theor) 249; m/z [M]+ 249 (using method, GC-MS Method 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09090632B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-146ab7320c0c43b1b23bae314d6c6779
출처 메모uspto-grants-2015_07