참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 4-(2-Benzyl-1,3-thiazol-4-yl)pyridine | HCID 14096952 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2-(p-Nitrobenzyl)-4-(4-pyridyl)thiazole | HCID 14096955 | 85.9% |
반응 단계
A solution of 2-benzyl-4-(4-pyridyl)thiazole (4.50 g, 0.018 mol) in chloroform (25 mL) was added dropwise to concentrated sulfuric acid (15 mL). The resulting mixture was cooled to 10° C. and fuming nitric acid (1.45 g, 0.97 mL) carefully added dropwise such that the reaction temperature did not exceed 40° C. The mixture was allowed to stir for thirty minutes, carefully neutralized with saturated sodium carbonate and the layers separated. The aqueous layer was reextracted with chloroform (2×25 mL) and the combined organic extracts were washed with brine (20 mL), dried over magnesium sulfate, and concentrated to afford a crude product (4.6 g). Several recrystallizations from hexane/ethyl acetate afforded pure 2-(p-nitrobenzyl)-4-(4-pyridyl)thiazole. mp. 140°-142° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04725606 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-ed73af56968b4454b488f0c1be5537e4 |
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| 출처 메모 | uspto-grants-1988_02 |
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