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Triethylamine → 3-Fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate

HRID 68253
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HRID 68253 반응식
[O:1]1[CH2:5][CH2:4][NH:3][C:2]1=[O:6].ClC(Cl)(O[C:11](=[O:17])[O:12][C:13](Cl)(Cl)Cl)Cl.C(N(CC)CC)C.[F:26][C:27]1[CH:34]=C(O)[CH:32]=[CH:31][C:28]=1[CH:29]=[O:30]>C(Cl)Cl.CC(OC)(C)C.O.C1COCC1>[O:6]=[C:2]1[N:3]([C:11]([O:12][C:13]2[CH:32]=[CH:31][C:28]([CH:29]=[O:30])=[C:27]([F:26])[CH:34]=2)=[O:17])[CH2:4][CH2:5][O:1]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 4

HCID 8471Triethylamine2회HCID 739492-OxazolidinoneHCID 94429TriphosgeneHCID 5872462-Fluoro-4-hydroxybenzaldehyde

생성물 1

HCID 582346863-Fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate수율 126%

시약·촉매·용매 4

HCID 962Water
용매
HCID 6344Dichloromethane용매
HCID 8028Tetrahydrofuran용매
HCID 15413tert-Butyl methyl ether용매

실험 절차

To a 250 mL dry round bottom flask were added 2-oxazolidinone (4.35 g, 50.0 mmol), triphosgene (5.49 g, 18.5 mmol) and anhydrous THF (100 mL). The mixture was stirred in an ice-water bath, then triethylamine (9.8 mL, 70.0 mmol) was added slowly. After stirring at 0° C. for 1 hour, the mixture was stirred continually at room temperature overnight. The reaction mixture was filtered and the filtrate was concentrated. The residue was dissolved in 10 mL of CH2Cl2, and this solution was added slowly to a stirring mixture of 2-fluoro-4-hydroxybenzaldehyde (3.78 g, 27.0 mmol) and triethylamine (5.63 mL, 40.4 mmol) in 20 mL of anhydrous CH2Cl2 at 0° C. After stirring at room temperature for 2 days, water (80 mL) and MTBE (100 mL) were added to the reaction mixture. The mixture was filtered and the solid was washed with cold water (50 mL×2), followed by extraction using MTBE (50 mL×4). After drying, 3-fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate (5.90 g) was obtained as a white solid. Yield: 86%. 1H NMR (CDCl3, 300 MHz): δ=10.42 (s, 1H), 8.03 (t, J=8.1 Hz, 1H), 7.27-7.23 (m, 2H), 4.61 (t, J=7.8 Hz, 2H), 4.29 (t, J=7.5 Hz, 2H). 13C NMR (CDCl3, 75.5 MHz): δ=186.3 (d, J=6.0 Hz), 166.9, 155.0 (d, J=260 Hz), 130.2, 122.6, 118.3, 110.7 (d, J=24.4 Hz), 62.2, 43.9. 19F NMR (CDCl3, 282.3 MHz): δ=−118.6.

후처리

  1. customTo a 250 mL dry round bottom flask
  2. stirringAfter stirring at 0° C. for 1 hour
  3. stirringthe mixture was stirred continually at room temperature overnight
  4. filtrationThe reaction mixture was filtered
  5. concentrationthe filtrate was concentrated
  6. dissolutionThe residue was dissolved in 10 mL of CH2Cl2
  7. stirringAfter stirring at room temperature for 2 days
  8. filtrationThe mixture was filtered
  9. washthe solid was washed with cold water (50 mL×2)
  10. extractionfollowed by extraction
  11. customAfter drying

출처 및 근거

ORD 기록
ord-1001e607261c4c708480e6eb3d2d7975
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822435B2

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