Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Hydroxide → 5-Amino-6-bromo-2-pyridinecarbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | 5-Aminopyridine-2-carbonitrile | HCID 3871395 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 5-Amino-6-bromo-2-pyridinecarbonitrile | HCID 24213892 | 35.9% |
반응 단계
5-Aminopyridine-2-carbonitrile (2.38 g, 20 mmol) was dissolved in 6 mL of glacial acetic acid. A solution of bromine (1 mL, 20 mmol) in 2.5 mL of glacial acetic acid was added dropwise over a period of 30 minutes while the room temperature was maintained with a water bath. The resulting slurry was stirred for 1 hour at room temperature, treated with 50 mL of aqueous 20% sodium hydroxide solution and extracted with three 160 mL portions of dichloromethane. The combined organic layers were dried over sodium sulfate (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by crystallization from ethyl acetate-hexanes to give 5-amino-6-bromopyridine-2-carbonitrile (1.42 g, 35% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08741897B2 |
| 출처 데이터셋 | uspto-grants-2014_06 |
| ORD ID | ord-3f12eec8677b4ebf8019de91e1881cd1 |
| 출처 메모 | uspto-grants-2014_06 |