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Methane → (S)-4-cyclohexyloxazolidin-2-one

HRID 539047
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HRID 539047 반응식
[O:1]=[C:2](Cl)[O:3][C:4](Cl)(Cl)Cl.[NH2:9][C@@H:10]([CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)CO.CCN(CC)CC.C>C1COCC1>[CH:13]1([C@H:10]2[CH2:4][O:3][C:2](=[O:1])[NH:9]2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1
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참가 물질

6

반응물 4

HCID 297MethaneHCID 8471TriethylamineHCID 10426DiphosgeneHCID 42614507(S)-2-Amino-2-cyclohexylethanol

생성물 1

HCID 58229227(S)-4-cyclohexyloxazolidin-2-one수율 87.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
50 °C

실험 절차

Diphosgene (0.704 mL, 6.05 mmol) was added dropwise to a stirred suspension of (S)-2-amino-2-cyclohexylethanol (1.02 g, 7.12 mmol), Et3N (6.95 mL, 49.9 mmol) and activated charcoal (40 mg) in THF (20 mL) at 0° C. under N2. The reaction mixture was heated at 50° C. overnight. After cooling, the suspension was filtered through Celite. To the filtrate was added sat. aq. NaHCO3 solution. The mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried and concentrated. The residue was purified by silica gel flash column chromatography (1:1 hexane/EtOAc) to give (S)-4-cyclohexyloxazolidin-2-one (0.900 g, 75%) as a white solid.

후처리

  1. temperatureAfter cooling
  2. filtrationthe suspension was filtered through Celite
  3. additionTo the filtrate was added sat. aq. NaHCO3 solution
  4. extractionThe mixture was extracted with EtOAc
  5. washThe combined organic layers were washed with brine
  6. customdried
  7. concentrationconcentrated
  8. customThe residue was purified by silica gel flash column chromatography (1:1 hexane/EtOAc)

출처 및 근거

ORD 기록
ord-4e5c8185a12e4909944874703c91166a
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865726B2

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