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HRID 549354作成日:2026年10月27日

Acetonitrile → tert-butyl (2S)-2-(2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/549354

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物DiisopropylethylamineHCID 81531—
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物(S)-2-(1-BOC-2-pyrrolidinyl)acetic acidHCID 688605—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl (2S)-2-(2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylateHCID 11075654—

反応手順

A solution of (S)-2-carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (2.00 g) in methanol (1.32 ml)/acetonitrile (40 ml) was treated with N,N-diisopropylethylamine (1.78 ml). Trimethylsilyldiazomethane (2M, 8.73 ml) was added dropwise and the resulting mixture was stirred at room temperature, under argon for 24 h. The mixture was diluted with ethyl acetate, washed with 2M HCl, saturated aqueous sodium hydrogen carbonate, brine then dried (magnesium sulfate). The solvent was removed under reduced pressure to afford the title compound (2.10 g)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943645B2
出典データセットuspto-grants-2011_05
ORD IDord-67ba47f2c0724598a71ab82276e2df3f
出典メモuspto-grants-2011_05