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Potassium Carbonate → (R)-(-)-5,5-Dimethyl-4-phenyl-2-oxazolidinone

HRID 2392833
ノート
印刷プレビュー

反応式

HRID 2392833 の反応式
[OH:1][C:2]([CH3:18])([CH3:17])[C@H:3]([NH:10][C:11](=[O:16])C(Cl)(Cl)Cl)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[C:4]1([C@@H:3]2[C:2]([CH3:18])([CH3:17])[O:1][C:11](=[O:16])[NH:10]2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 11430Potassium CarbonateHCID 67618536HCID 67618536、化合物

生成物 1

HCID 6950851(R)-(-)-5,5-Dimethyl-4-phenyl-2-oxazolidinone収率 92.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of (14) (1.655 g, 5.33 mmol) in ethanol (140 ml) was added potassium carbonate (0.369 g. 2.67 mmol) and the solution was refluxed for 30 minutes. After concentration in vacuo, dichloromethane was added and the mixture was washed with saturated aqueous sodium chloride solution. Concentration in vacuo gave crude crystalline solid which was purified by recrystallisation in ethyl acetate/pentane to give the title compound (15) (0.939 g, 92%); mp 149° C.; νmax (CHCl3) 1753 cm-1 ; [α]D25 (c 0.5 in CHCl3)=-77.6; (Found: C, 69.32; H, 7.05; N, 7.38. C11H13NO2 requires C, 69.09; H, 6.85; N, 7.33%); δH (200 MHz; CDCl3) 0.93 (3H, s, C(CH3)2), 1.61 (3H, s, C(CH3)2), 4.66 (1H, s, CHPh), 6.25 (1H, s, NH), 7.25-7.44 (5H, m, ArCH); δC (125 MHz; CDCl3 23.53 (CH3), 28.04 (CH3), 65.93 (CH), 84.63 (C), 126.67 (ArCH), 128.72 (ArCH), 128.93 (ArCH), 137.16 (C), 159.75 (CO) ; m/z (CI+, NH3) 192 (M+ +1).

後処理

  1. temperaturethe solution was refluxed for 30 minutes
  2. concentrationAfter concentration in vacuo, dichloromethane
  3. additionwas added
  4. washthe mixture was washed with saturated aqueous sodium chloride solution
  5. concentrationConcentration in vacuo
  6. customgave crude crystalline solid which
  7. customwas purified by recrystallisation in ethyl acetate/pentane

出典と根拠

ORDレコード
ord-6366aaf1f9b04914ab60a33187a60c25
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05801249

反応ノート

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