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

HRID 539047
ノート
印刷プレビュー

反応式

HRID 539047 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 58229227(S)-4-cyclohexyloxazolidin-2-one収率 87.9%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
50 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-4e5c8185a12e4909944874703c91166a
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08865726B2

反応ノート

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