Tetrahydrofuran → 3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactam

HRID 892620

반응식

HRID 892620 반응식
ClC([O:4][CH2:5][CH3:6])=O.O[C:8]1[CH:9]=[C:10]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[CH:11]=[CH:12][C:13]([OH:15])=O.C(N(CC)CC)C.[NH2:28][CH:29]1[CH2:36][CH2:35][CH2:34][NH:33][C:31](=[O:32])[CH2:30]1.C1C[O:40]CC1>>[CH2:5]([O:4][C:20]([O:19][C:18]1[CH:8]=[CH:9][C:10]([CH:11]=[CH:12][C:13]([NH:28][CH:29]2[CH2:36][CH2:35][CH2:34][NH:33][C:31](=[O:32])[CH2:30]2)=[O:15])=[CH:16][CH:17]=1)=[O:40])[CH3:6]

참가 물질

6

실험 절차

Ethyl chloroformate (22.2 ml) was added dropwise to a mixture of 3-hydroxy-4-methoxycinnamic acid (22.5 g), triethylamine (32.3 ml) and THF (400 ml) under ice-cooling and stirring, followed by stirring for 15 mins. Subsequently, to the mixture was added dropwise a solution of 3-amino-ε-caprolactam (14.9 g) in THF (200 ml), and then the whole was stirred for 1 hr. at room temperature. After completing the dropping, the reaction mixture was concentrated under reduced pressure, and the residue was dissolved in chloroform. This solution was washed with water, dried and distilled under reduced pressure to remove the solvent. The residue was washed with ethyl acetate, dried under reduced pressure to give the title compound (28 g). This compound was used in the following reaction without purification.

후처리

  1. temperaturecooling
  2. stirringby stirring for 15 mins
  3. stirringthe whole was stirred for 1 hr
  4. customat room temperature
  5. concentrationwas concentrated under reduced pressure
  6. dissolutionthe residue was dissolved in chloroform
  7. washThis solution was washed with water
  8. customdried
  9. distillationdistilled under reduced pressure
  10. customto remove the solvent
  11. washThe residue was washed with ethyl acetate
  12. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-2f7299906dbe4a1e92167c16c3c5d7ce
출처 데이터셋
uspto-grants-1992_06
특허 번호
US05118806

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