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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1330생성일: 2026년 10월 23일

Pyridine → 1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylate

https://huagongshe.com/ko/reaction/1330

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzyl chloroformateHCID 10387—
반응물tert-Butyl pyrazolidine-3-carboxylateHCID 57015512—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물1-Benzyl 3-tert-butyl 1,3-pyrazolidinedicarboxylateHCID 13341540—

반응 조건

온도0 °C

반응 단계

A solution of 3-pyrazolidinecarboxylic acid, 1,1-dimethylethyl ester (10.935 g., 63.5 mmol.) in dry acetonitrile (90 ml.) was cooled to 0° C. (ice-salt bath) and treated with dry pyridine (11.0 ml.) followed by a solution of benzylchloroformate (12.54 g., 10.5 ml., 69.9 mmol.) in dry acetonitrile (25 ml.). The reaction was stirred at 0° C. for 3 hours, evaporated to dryness and the syrup obtained was redissolved in ethyl acetate (250 ml.). The solution was washed with 5% sodium bicarbonate (2×25 ml.) and brine (25 ml.), dried (anhydrous sodium sulfate), filtered, evaporated to dryness and dried in vacuo. The crude product mixture was chromatographed on a silica gel column (Merck), eluting the column with ethyl acetate:hexane mixtures (1:4; 1:2) to give 11.144 g. of title product as a syrup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723602
출처 데이터셋uspto-grants-1998_03
ORD IDord-8a9fc26c3201445093ccc42bd50dbc2c
출처 메모uspto-grants-1998_03