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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60575생성일: 2026년 10월 24일

1,2-Dibromoethane → Tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/60575

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DibromoethaneHCID 7839—
반응물Ammonium ChlorideHCID 25517—
반응물4-Bromobenzyl bromideHCID 68527—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물Tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 7085143740.4%

반응 단계

To a suspension of magnesium (2.9 g) in diethyl ether (50 mL) was added dropwise 1,2-dibromoethane (0.90 mL) at room temperature, and the reaction mixture was vigorously stirred at room temperature for 20 min. To the reaction mixture was added dropwise a solution of 4-bromobenzyl bromide (25 g) in diethyl ether (150 mL) over 30 min or more at 0° C., and then added dropwise a solution of tert-butyl 4-oxopiperidine-1-carboxylate (16 g) in diethyl ether (200 mL) over 30 min or more 0° C. The reaction mixture was allowed to warm to room temperature, and stirred at room temperature for 3 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution (200 mL), and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (12 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440990B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-dba157cd4aee4c5faa3e18ea51cfbaaf
출처 메모uspto-grants-2016_09