참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phosphorus tribromide | HCID 24614 | — |
| 반응물 | 5-Hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine | HCID 70419877 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine | HCID 10430078 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04727073 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-5445957897b14e47a375be80f7ca2538 |
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| 출처 메모 | uspto-grants-1988_02 |
|---|