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HRID 1057854作成日:2026年10月26日

Hydantoin → 3-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-4-methoxybenzylidene-2,4-imidazolidinedione

https://huagongshe.com/reaction/1057854

反応式

関与物質

役割名称HCID仕込み量
反応物HydantoinHCID 10006—
反応物PyrrolidineHCID 31268—
反応物3-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methoxy-benzaldehydeHCID 11279126—
溶媒EthanolHCID 702—
生成物3-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-4-methoxybenzylidene-2,4-imidazolidinedioneHCID 69462356—

反応手順

A mixture of 2,4-imidazolidinedione (101 mg, 1.0 mmol), pyrrolidine (0.04 mL, 0.5 mmol) and 3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4-methoxy-benzaldehyde (336 mg, 1.0 mmol) in ethanol (15 mL) was heated under reflux for 24 hours, allowed to cool to room temperature and extracted with ethyl acetate (2×100 mL). The organic extracts were washed with saturated aqueous NH4Cl (60 mL), saturated NH4Cl (70 mL), saturated aqueous NaCl (60 mL), dried over MgSO4 and filtered. Removal of the solvent under reduced pressure gave a yellow solid that was purified by column chromatography, using a Biotage 40S cartridge, eluting with ethyl acetate/hexane (3:7). The title compound was isolated as a yellow solid (270 mg, 65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06515003B1
出典データセットuspto-grants-2003_02
ORD IDord-5fabd2b7efdb48fda4fed3e0158d4148
出典メモuspto-grants-2003_02