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HRID 1805237作成日:2026年10月27日

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

https://huagongshe.com/reaction/1805237

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物(RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 67151644—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
生成物(RS)-4-(4-cyano-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6715163955%

反応手順

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]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08354441B2
出典データセットuspto-grants-2013_01
ORD IDord-99793e271f9046a3abb2050b00126617
出典メモuspto-grants-2013_01