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HRID 4676作成日:2026年10月24日

Sodium borohydride → 5-(1-Hydroxyethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine

https://huagongshe.com/ja/reaction/4676

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物5-Acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidineHCID 15147477—
溶媒MethanolHCID 887—
生成物5-(1-Hydroxyethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidineHCID 2015139776.2%

反応手順

A mixture of 5-acetyl-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (3 g) and sodium borohydride (0.34 g) in methanol (110 ml) was stirred at room temperature for 4 hours. The reaction mixture was evaporated in vacuo and the residue was poured into a mixture of ethyl acetate and water. The separated organic layer was dried over magnesium sulfate and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of n-hexane and diethyl ether to give a 5-(1-hydroxyethyl)-6-methyl-4-(3-nitrophenyl)-2-phenylpyrimidine (2.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727073
出典データセットuspto-grants-1988_02
ORD IDord-85ec00ae73394616852dbd4678f08fe0
出典メモuspto-grants-1988_02