참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Phosphorus tribromide | HCID 24614 | — |
| 반응물 | HCID 178428770 | HCID 178428770 | — |
| 용매 | Dimethylformamide toluene | HCID 21735183 | — |
| 생성물 | 2-Bromo-3-methyl-5-nitropyridine | HCID 5200466 | 99% |
반응 단계
A sample of 3-methyl-5-nitropyridin-2-ol (1.44 g, 9.34 mmol) was placed in 35 mL pressure vessel and dissolved in a mixture of toluene/DMF (10:1 ratio; 15 mL). The vessel was capped with a septum, flushed with Argon and phosphorous tribromide (1.32 mL, 14.0 mmol) was added by syringe. The septum cap was replaced by a Teflon cap and the mixture was stirred for 20 min at 120° C. The mixture was cooled to room temperature, neutralized with a 3M NaOH solution and extracted with toluene (3×). The combined organic phases were dried over anhydrous MgSO4 and concentrated under vacuum to give 2.00 g of the desired 2-bromo-3-methyl-5-nitropyridine product as an orange solid (99%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09290526B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-5404c3f467f74576a0a014c0987fa628 |
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| 출처 메모 | uspto-grants-2016_03 |
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