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Potassium Carbonate → (S)-4,5,5-Trimethyloxazolidin-2-one

HRID 2392824
ノート
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反応式

HRID 2392824 の反応式
[OH:1][C:2]([CH3:13])([CH3:12])[C@@H:3]([NH:5][C:6](=[O:11])C(Cl)(Cl)Cl)[CH3:4].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH3:4][C@H:3]1[C:2]([CH3:13])([CH3:12])[O:1][C:6](=[O:11])[NH: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 86753059N-[(1S)-2-Hydroxy-1,2-dimethylpropyl]-2,2,2-trichloroethanamide

生成物 1

HCID 11073445(S)-4,5,5-Trimethyloxazolidin-2-one

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of (4) (1.964 g, 7.92 mmol) in ethanol (140 ml) was added potassium carbonate (0.547 g, 3.96 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 toluene/60-80 petroleum ether giving the title compound (5) (0.968 g, 95%); mp 60° C.; νmax (CDCl3) 1758 cm-1 ; [α]D24 (c 2 in CHCl3)=+1.2; (Found: C, 56.13; H, 8.85; N, 10.79. C6H11NO2 requires C, 55.80; H, 8.58; N, 10.84%); δH (500 MHz; CDCl3) 1.12 (3H, d, J=6.6, CHCH3), 1.27 (3H, s, C(CH3)2), 1.39 (3H, s, C(CH3)2), 3.59 (1H, J=6.5, CHCH3), 7.27 (1H, s, NH); δC (125 MHz; CDCl3) 16.07 (CH3), 21.46 (CH3), 27.14 (CH3), 57.12 (CH), 83.50 (C), 159.00 (CO); m/z (CI+, NH3) 130 (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
  5. concentrationConcentration in vacuo
  6. customgave crude crystalline solid which
  7. customwas purified by recrystallisation in toluene/60-80 petroleum ether giving the title compound (5) (0.968 g, 95%)

出典と根拠

ORDレコード
ord-52b96f605d814e1f9eca453bc375883e
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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