戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2257115作成日:2026年10月27日

Diethyl (ethoxymethylene)malonate → Ethyl 4-hydroxy-2-methylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/2257115

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (ethoxymethylene)malonateHCID 6871—
反応物Ethanimidamide, acetate (1:1)HCID 160356—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 4-hydroxy-2-methylpyrimidine-5-carboxylateHCID 29375046%

反応手順

Acetamidine acetate (37.21 g, 0.31 mole) and diethyl ethoxymethylenemalonate (63 mL, 0.31 mole) were refluxed for 4 h in ethanol (60 mL). The reaction mixture was allowed to cool for 15 min., then acetamidine acetate (37.21 g, 0.31 mole) was added. The reaction mixture was refluxed for 22 hours, allowed to cool to room temperature, and diluted with water (200 mL) and dichloromethane (200 mL). The aqueous layer was extracted with 10% isopropanol/dichloromethane (2×200 mL). The combined organic extracts were washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered and the solvent was removed. The residue was recrystallized from chloroform/hexanes in two crops to afford the title compound (24.92 g) in 46% yield as yellowish crystals. Rf =0.27 (silica gel, 10% isopropanol in dichloromethane). m.p. 187°-188° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05656645
出典データセットuspto-grants-1997_08
ORD IDord-e0b8184e6eba483189c7564e33c8ae02
出典メモuspto-grants-1997_08