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Triethylamine → 3-(2,6-Dimethylphenyl)-1-ethyl-2-thioxo-imidazolidin-4-one

HRID 343600
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HRID 343600 반응식
[CH2:1]([NH:3][CH2:4][C:5]([OH:7])=O)[CH3:2].[CH3:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:10]=1[N:16]=[C:17]=[S:18].C(N(CC)CC)C>C(Cl)Cl>[CH3:15][C:11]1[CH:12]=[CH:13][CH:14]=[C:9]([CH3:8])[C:10]=1[N:16]1[C:5](=[O:7])[CH2:4][N:3]([CH2:1][CH3:2])[C:17]1=[S:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 879762,6-Xylyl isothiocyanateHCID 316542N-Ethylglycine

생성물 1

HCID 114365903-(2,6-Dimethylphenyl)-1-ethyl-2-thioxo-imidazolidin-4-one수율 18.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of N-ethyl glycine (9.2 g), 2,6-dimethylphenyl-isothiocyanate (8.2 g), triethylamine (10.1 g), and methylene chloride (150 mL) was heated at reflux for 3.5 hours. The mixture was evaporated to dryness. Purification was achieved through crystallization from ethanol. The title compound (2.3 g) was obtained as a white solid (2.3 g). m.p. 128°-131° C. Anal. Calcd. for. C13H16N2OS: C, 62.87; H, 6.49; N, 11.28. Found: C, 62.83; H, 6.50; N, 11.25. Mass spectrum (EI, M.+) m/z 248.

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후처리

  1. temperaturewas heated
  2. temperatureat reflux for 3.5 hours
  3. customThe mixture was evaporated to dryness
  4. customPurification
  5. customwas achieved through crystallization from ethanol

출처 및 근거

ORD 기록
ord-497f500330044158bb46447d68ff46cf
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05861517

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