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HRID 30645作成日:2026年10月25日

3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione → 5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dione

https://huagongshe.com/reaction/30645

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dioneHCID 1482884—
触媒HCID 178418390HCID 178418390—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dioneHCID 276837379.4%

反応手順

A mixture of 3-methyl-5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione (1.0 g), 5% palladium carbon (1.0 g) and tetrahydrofuran (150 mL) was subjected to catalytic reduction under hydrogen pressure of 5.0 kgf·cm−2. The catalyst was removed by filtration, and the filtrate was concentrated to give 5-(4-aminobenzyl)-3-methyl-1,3-thiazolidine-2,4-dione as colorless crystals (0.71 g, yield 79%). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 91-92° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-45c08b9c0289483abe2788e113b3c415
出典メモuspto-grants-2008_09