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Phosphorus oxybromide → 2-Bromo-5-methyl-3-nitropyridine

HRID 1054494
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인쇄 미리보기

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HRID 1054494 반응식
P(Br)(Br)([Br:3])=O.O[C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[CH:11][C:10]([CH3:16])=[CH:9][N:8]=1>CN(C=O)C>[Br:3][C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[CH:11][C:10]([CH3:16])=[CH:9][N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24613Phosphorus oxybromideHCID 178430719HCID 178430719, 화합물

생성물 1

HCID 123624472-Bromo-5-methyl-3-nitropyridine수율 86%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
5 °C

실험 절차

POBr3 (222.8 g, 0.78 mol) was added in portions to 2-hydroxy-5-methyl-3-nitropyridine (100 g, 0.65 mol) in DMF (500 mL) with stirring at 0-10° C. then the reaction mixture was stirred at 80° C. under nitrogen for 12 hours. Reaction mixture was cooled and poured into crushed ice (1 Kg), obtained solid was filtered, washed thoroughly with ice-cold water (2×500 mL), dried in a desiccator under high vacuum for one day to obtain 2-bromo-5-methyl-3-nitropyridine as yellow solid (121 g) in 86% yield. (M+H) Expected: 217. found 216.9.

후처리

  1. stirringthe reaction mixture was stirred at 80° C. under nitrogen for 12 hours
  2. customReaction mixture
  3. temperaturewas cooled
  4. additionpoured
  5. customobtained solid
  6. filtrationwas filtered
  7. washwashed thoroughly with ice-cold water (2×500 mL)
  8. customdried in a desiccator under high vacuum for one day

출처 및 근거

ORD 기록
ord-6234d377ee1447bab1166a30dc349585
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394307B2

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