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HRID 16038作成日:2026年10月24日

tert-butyl N-(4-aminobutyl)carbamate → 1-(4-N-Boc-aminobutyl)-1H-pyrrole-2,5-dione

https://huagongshe.com/ja/reaction/16038

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
反応物Maleic AnhydrideHCID 7923—
溶媒TolueneHCID 1140—
生成物1-(4-N-Boc-aminobutyl)-1H-pyrrole-2,5-dioneHCID 59709139—

反応手順

To a solution of N-BOC-1,4-diaminobutane (8.324 g, 0.044 mol) in dry toluene (50 ml) was added maleic anhydride (4.336 g, 0.044 mol) and the solution heated at reflux under Dean-Stark conditions for two days. The solvent was removed and the residue purified by silica column chromatography eluting with 25-40% ethyl acetate in hexane to give the title compound, 1.461 g, 12%, as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07736635B2
出典データセットuspto-grants-2010_06
ORD IDord-5f8e5d07e27c4cbb8e72a0fb83256796
出典メモuspto-grants-2010_06