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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1805237생성일: 2026년 10월 26일

Dimethylformamide → (RS)-4-(4-cyano-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1805237

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물(RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 67151644—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
생성물(RS)-4-(4-cyano-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6715163955%

반응 단계

A stirred solution of (RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (200 mg, example 1(e)), zinc cyanide (66 mg) and tetrakis(triphenyl-phosphine)palladium (57 mg) in DMF (4 ml) under an argon atmosphere in a sealed tube was heated at 160° C. for 15 minutes under microwave irradiation. The mixture was then poured onto ice-water and the mixture extracted twice with ethyl acetate. The combined organic extracts were washed with water, dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (SiO2; gradient: heptane/EtOAc) to give (RS)-4-(4-cyano-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (82 mg, 55%) as a colourless viscous oil. MS (ISP): 325.4 ([M+Na]+), 303.4 ([M+H]+), 247.3 ([M+H—C4H8]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354441B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-99793e271f9046a3abb2050b00126617
출처 메모uspto-grants-2013_01