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HRID 255732作成日:2026年10月27日

5-Acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine → 6-Methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylic acid

https://huagongshe.com/reaction/255732

反応式

関与物質

役割名称HCID仕込み量
反応物5-Acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidineHCID 15147477—
反応物Sodium BisulfiteHCID 23665763—
反応物Sodium hypobromiteHCID 23673712—
溶媒TetrahydrofuranHCID 8028—
生成物6-Methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylic acidHCID 15147487—

反応手順

A mixture of 5-acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (1.5 g), tetrahydrofuran (70 ml), sodium hypobromite (70 ml) was stirred for 2 hours at ambient temperature. To the mixture was added an aqueous sodium bisulfite solution. The mixture was washed with diethyl ether (100 ml) and the aqueous solution was acidified to pH 3.0 with 10% hydrochloric acid. The resultant crystals were collected by filtration to give 0.80 g of 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04698340
出典データセットuspto-grants-1987_10
ORD IDord-19c85a267351462d806f23799a5721f5
出典メモuspto-grants-1987_10