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HRID 917384作成日:2026年10月26日

Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester → Ethyl 2-benzyl-4-methylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/917384

反応式

関与物質

役割名称HCID仕込み量
反応物Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
反応物Sodium AcetateHCID 517045—
反応物2-Phenylethanimidamide hydrochlorideHCID 12415514—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 2-benzyl-4-methylpyrimidine-5-carboxylateHCID 1219476989%

反応条件

温度100 °C

反応手順

To 100 ml of N,N-dimethylformamide, 17.1 g (100 mmol) of 2-phenylacetoamidine hydrochloric acid salt, synthesized in accordance with a method described in “Tetrahedron”, page 887 (1984), 18.6 g (100 mmol) of ethyl 2-acetyl-3-ethoxyacrylate and 9.0 g (110 mmol) of sodium acetate were suspended, followed by stirring at 100° C. for 3 hours. The reaction liquid was cooled and then poured into ice water, and extracting with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 22.8 g (yield: 89%) of ethyl 2-benzyl-4-methylpyrimidine-5-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07273878B2
出典データセットuspto-grants-2007_09
ORD IDord-22aa77e03b3042448a53c53288fa8fe5
出典メモuspto-grants-2007_09