Sodium Hydroxide → phenyl N-[3-(dimethylcarbamoyl)phenyl]carbamate

HRID 864564노트

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HRID 864564 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[C:5]([N:7]([CH3:9])[CH3:8])=[O:6].[OH-].[Na+].Cl[C:16]([O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:17]>O1CCOCC1>[CH3:8][N:7]([CH3:9])[C:5]([C:4]1[CH:3]=[C:2]([NH:1][C:16](=[O:17])[O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:12]=[CH:11][CH:10]=1)=[O:6]

참가 물질

5

실험 절차

To a stirred solution of 3-amino-N,N-dimethylbenzamide (1.3 g) in 1,4-dioxane(20 ml) was added 1N sodium hydroxide (23.4 ml) and phenyl chloroformate (1.5 ml) successively in an ice-cooled bath. The bath was removed and the reaction mixture was stirred vigorously for 3 hours during which time, phenyl chloroformate (0.7 ml) was further added. The mixture was extracted with ethyl acetate and the organic layer was washed with water and saturated sodium chloride solution. After dried over anhydrous magnesium sulfate and filtered, the solvent was removed in vacuo and the residual oil was purified by flash chromatography eluting with ethyl acetate-n-hexane (2:1, V/V) to give a solid, which was recrystallized from benzene-n-hexane (5:1, V/V) to afford phenyl 3-(dimethylcarbamoyl)phenylcarbamate (1.4 g) as a colorless powder.

후처리

  1. temperaturecooled bath
  2. customThe bath was removed
  3. additionwas further added
  4. extractionThe mixture was extracted with ethyl acetate
  5. washthe organic layer was washed with water and saturated sodium chloride solution
  6. dry with materialAfter dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customthe solvent was removed in vacuo
  9. customthe residual oil was purified by flash chromatography
  10. washeluting with ethyl acetate-n-hexane (2:1, V/V)
  11. customto give a solid, which
  12. customwas recrystallized from benzene-n-hexane (5:1, V/V)

출처 및 근거

ORD 기록
ord-8473e907ab6c4ce0bc76ec05760c7a36
출처 데이터셋
uspto-grants-1996_10
특허 번호
US05563162

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