関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Phosphorus tribromide | HCID 24614 | — |
| 反応物 | 5-Hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine | HCID 70419877 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04727073 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-5445957897b14e47a375be80f7ca2538 |
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| 出典メモ | uspto-grants-1988_02 |
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