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HRID 457919作成日:2026年10月26日

proline dl-form → 1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/457919

反応式

関与物質

役割名称HCID仕込み量
反応物proline dl-formHCID 614—
反応物MethanolHCID 887—
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物(2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acidHCID 58714586—
溶媒TolueneHCID 1140—
生成物1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylateHCID 58585478—

反応手順

A solution of the oximether- and/or olefin-type 2-pyrrolidinecarboxylic acid intermediate, e.g. (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid (0.648 g, 2.5 mmol), in a 1:1 mixture of methanol and toluene (35 ml) was made. Trimethylsilyl diazomethane (3.8 ml of a 2M solution in hexanes, 7.5 mmol) was then added dropwise to the stirred solution at room temperature under nitrogen. After completion of the evolution of nitrogen gas, the resulting yellow solution was evaporated in vacuo, and the residue filtered through a pad of silica gel, eluting with ethyl acetate. Removal of solvent from the filtrate gave the methylester product, e.g. 1-tert-butyl 2-methyl(2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate, as a yellow oil (0.646 g, 95% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189754B2
出典データセットuspto-grants-2007_03
ORD IDord-d1b970716bbc4b3c94fe462585b988e2
出典メモuspto-grants-2007_03