Hydrochloric Acid → N-Ethyl-2-hydroxybenzamide

HRID 553258

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HRID 553258 반응식
[CH:1]1[CH:2]=[CH:3][C:4]2[O:12][C:10](=O)[NH:9][C:7](=[O:8])[C:5]=2[CH:6]=1.[C:13](=O)([O-])[O-].[Na+].[Na+].ICC.[OH-].[Na+].Cl>CC(N(C)C)=O>[CH2:10]([NH:9][C:7](=[O:8])[C:5]1[C:4](=[CH:3][CH:2]=[CH:1][CH:6]=1)[OH:12])[CH3:13]

참가 물질

7

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온도
80 °C

실험 절차

Dimethylacetamide (50 ml) and carsalam (10.00 g, 0.0613 mol) were placed into a round bottom flask fitted with nitrogen purge, cold water condenser and a magnetic stir bar. Sodium carbonate (6.50 g, 0.0613 mol) and iodoethane (4.38 ml, 0.0548 mol) were added and heating of the reaction mixture was started. Heating at 80° C. continued for 16 hours at which point heating was discontinued and the reaction mixture was allowed to cool to room temperature. The reaction mixture was then filtered through a sintered glass funnel and the filtrate was collected. Water was added to this filtrate until a white solid precipitated. The solid was isolated by filtration and placed in an Erlenmeyer flask with 2N aqueous sodium hydroxide solution (200 ml). This mixture was heated at reflux for approximately 1 hour and then stirred overnight at room temperature. This mixture was acidified with 2N aqueous hydrochloric acid and a yellow oil was noted to separate out. The reaction mixture was extracted two times with 200 ml portions of ethyl acetate. The combined ethyl acetate layers were washed two times with 200 ml portions of deionized water, dried with sodium sulfate and concentrated under vacuum. N-ethylsalicylamide was recovered as a yellow oil which, after drying overnight under vacuum, was isolated in a yield of 7.93 g.

후처리

  1. customfitted with nitrogen
  2. custompurge
  3. temperatureheating of the reaction mixture
  4. temperatureheating
  5. temperatureto cool to room temperature
  6. filtrationThe reaction mixture was then filtered through a sintered glass funnel
  7. customthe filtrate was collected
  8. additionWater was added to this filtrate until a white solid
  9. customprecipitated
  10. customThe solid was isolated by filtration
  11. temperatureThis mixture was heated
  12. temperatureat reflux for approximately 1 hour
  13. customto separate out
  14. extractionThe reaction mixture was extracted two times with 200 ml portions of ethyl acetate
  15. washThe combined ethyl acetate layers were washed two times with 200 ml portions of deionized water
  16. dry with materialdried with sodium sulfate
  17. concentrationconcentrated under vacuum
  18. customN-ethylsalicylamide was recovered as a yellow oil which
  19. customafter drying overnight under vacuum
  20. customwas isolated in a yield of 7.93 g

출처 및 근거

ORD 기록
ord-378a03b477384841b01afaae366208de
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07951971B1

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