Hydrochloric Acid → 3-n-Hexyl-5-methylbromobenzene

HRID 522424

반응식

HRID 522424 반응식
Br[C:2]1[CH:3]=[C:4]([CH3:9])[CH:5]=[C:6]([Br:8])[CH:7]=1.Cl>O1CCCC1>[CH2:4]([C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([CH3:9])[CH:3]=1)[CH2:3][CH2:2][CH2:7][CH2:6][CH3:5]

참가 물질

4

반응 조건

온도
57 °C

실험 절차

After adding anhydrous tetrahydrofuran (2 L), 3,5-dibromotoluene (477 g, 1.91 mol) and 1,1-bis(diphenylphosphino)ferrocene dichloropalladium(II) dichloromethane complex (Pd(dppf).CH2Cl2, CAS:851232-71-8, 6.24 g, 7.64 mol) in a 6 L flask under an inert gas atmosphere, the mixture was stirred at 57° C. for 15 minutes. Next, solution 1-1 was added dropwise at rate which maintained a temperature of no higher than 60° C., and the mixture was stirred at 57° C. for 2 hours. The reaction mixture was then added to 10 wt % hydrochloric acid that had been cooled with an ice bath, and stirred, and extraction was performed with toluene. The obtained organic layer was rinsed twice with water and the organic layer was concentrated under reduced pressure to remove the solvent. This was followed by vacuum distillation and purification by column chromatography, to obtain 326 g of the target 3-n-hexyl-5-methylbromobenzene (compound 1-1 represented by the following formula).

후처리

  1. temperaturemaintained a temperature of no higher than 60° C.
  2. stirringthe mixture was stirred at 57° C. for 2 hours
  3. temperaturehad been cooled with an ice bath
  4. stirringstirred
  5. extractionextraction
  6. washThe obtained organic layer was rinsed twice with water
  7. concentrationthe organic layer was concentrated under reduced pressure
  8. customto remove the solvent
  9. distillationThis was followed by vacuum distillation and purification by column chromatography

출처 및 근거

ORD 기록
ord-df3608c19f2649329cb64464e428c66e
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09331284B2

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