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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1396894생성일: 2026년 10월 26일

Benzyl chloroformate → 1-Benzyl 2,3-di-tert-butyl pyrazolidine-1,2,3-tricarboxylate

https://huagongshe.com/reaction/1396894

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물Potassium CarbonateHCID 11430—
반응물Di-tert-butyl pyrazolidine-1,5-dicarboxylateHCID 68287714—
용매AcetonitrileHCID 6342—
생성물1-Benzyl 2,3-di-tert-butyl pyrazolidine-1,2,3-tricarboxylateHCID 8670633974.4%

반응 단계

Sat. aq. K2CO3 (210 mL) was added into a solution of benzyl chloroformate (12.0 ml, 84 mmol) and crude di-tert-butyl pyrazolidine-1,5-dicarboxylate (12.74 g, assumed 46.8 mmol) in acetonitrile (137 ml) at 0° C. The reaction was allowed to warm to room temperature and was stirred for 4.5 hrs. The aqueous phase was extracted with EtOAc (3×100 mL), and the organic layers were dried over Na2SO4. The solvents were removed in vacuo, and the crude product was purified by silica gel chromatography (CombiFlash, Column: 220 g; 0-35% ethyl acetate in hexane; 60 min) to provide the desired product 1-benzyl 2,3-di-tert-butyl pyrazolidine-1,2,3-tricarboxylate (14.15 g, 74% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901119B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-6daca42062404ff39d7acda688055210
출처 메모uspto-grants-2014_12