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HRID 4673作成日:2026年10月23日

Tetrahydrofuran → 5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine

https://huagongshe.com/ja/reaction/4673

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Potassium CarbonateHCID 11430—
反応物Phosphorus tribromideHCID 24614—
反応物5-Hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidineHCID 70419877—
溶媒BenzeneHCID 241—
生成物5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidineHCID 10430078—

反応手順

To a solution of phosphorus tribromide (16.85 g) in a mixture of benzene (150 ml) and tetrahydrofuran (150 ml) was dropwise added a solution of 5-hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine (30 g) in tetrahydrofuran (150 ml) under cooling at 7°-10° C. After stirring for 4 hours at the same temperature, the reaction mixture was poured into ice-water (200 ml), adjusted to pH 9.5 with saturated potassium carbonate and extracted with ethyl acetate (300 ml). After filtering off an insolble material, the organic layer was washed with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from diethyl ether to give 5-bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine (29.08 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-5445957897b14e47a375be80f7ca2538
出典メモuspto-grants-1988_02