Hydrogen Bromide → 2,5-Dibromo-4-methylpyridine

HRID 448851

반응식

HRID 448851 반응식
N[C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([Br:9])=[CH:4][N:3]=1.[BrH:10].BrBr.N([O-])=O.[Na+].[OH-].[Na+]>O.CCOCC.CCCCCC>[Br:10][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([Br:9])=[CH:4][N:3]=1

참가 물질

8

반응 조건

온도
2 °C

실험 절차

2-Amino-5-bromo-4-methylpyridine (2.0 g, 10.7 mmol) was dissolved in 48% aqueous HBr (14 mL, 123 mmol) and cooled to 2° C. in a salt/ice bath. Bromine (1.65 mL, 32.1 mmol) was added dropwise keeping the internal temperature below 2° C. A solution of sodium nitrite (3.69 g, 53.5 mmol) in water (5 mL) was added keeping the internal temperature below 5° C. and stirred for 1 h between 0° C. and 5° C. The pH was adjusted to ˜13 by slow addition with cooling of 50% NaOH (aq). After warming to r.t. the reaction was extracted with ether, the organics were dried over MgSO4 and concentrated to give a brown oil. Flash chromatography on silica gel eluting with 5% ether/hexane gave the product as a white solid (1.83 g, 7.29 mmol, 68%). MS [M+H]+: 251.9; tR=2.3 min. (method 1)

후처리

  1. customthe internal temperature below 2° C
  2. customthe internal temperature below 5° C.
  3. additionThe pH was adjusted to ˜13 by slow addition
  4. temperatureAfter warming to r.t. the reaction
  5. extractionwas extracted with ether
  6. dry with materialthe organics were dried over MgSO4
  7. concentrationconcentrated
  8. customto give a brown oil

출처 및 근거

ORD 기록
ord-238ee90e5be9455faff1967b03e285a4
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08481738B2

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