Ethanol → 5-Ethyl-5-(pentan-2-yl)imidazolidine-2,4-dione

HRID 1834891

反応式

HRID 1834891 の反応式
[C:1](=[O:4])([O-])[O-].[NH4+:5].[NH4+:6].[C-:7]#N.[Na+].C[CH:11]([CH2:17][CH3:18])[CH2:12][C:13](=O)[CH2:14][CH3:15].C(Cl)(Cl)Cl.[CH2:23]([OH:25])C>O>[CH:12]([C:11]1([CH2:17][CH3:18])[NH:6][C:23](=[O:25])[NH:5][C:1]1=[O:4])([CH2:13][CH2:14][CH3:15])[CH3:7]

参加物

7

反応条件

温度
55 °C

実験手順

To a slurry of ammonium carbonate (865 parts), sodium cyanide (180 parts) in water (1200 parts) was added 5-methyl-3-heptanone (385 parts) in ethanol (1200 parts) at ambient temperature with stirring. The reaction mixture was heated to 55° C over a period thirty minutes and maintained at 55° C for 6 hours. After cooling to ambient temperature, chloroform (1000 parts) was added and the mixture stirred for ten minutes. The reaction mixture was filtered and the filter cake washed with additional chloroform (500 parts). The organic phase was collected and the aqueous phase washed with additional chloroform (1000 parts) in two portions. The combined organic phase was evaporated to dryness yielding crude product. The resultant white solid was slurried in water (2000 parts), filtered and dried to constant weight to afford 5-sec-amyl-5-ethylhydantoin (560 parts, 94% yield, mp 151°-6° C.

後処理

  1. temperaturemaintained at 55° C for 6 hours
  2. temperatureAfter cooling to ambient temperature
  3. stirringthe mixture stirred for ten minutes
  4. filtrationThe reaction mixture was filtered
  5. washthe filter cake washed with additional chloroform (500 parts)
  6. customThe organic phase was collected
  7. washthe aqueous phase washed with additional chloroform (1000 parts) in two portions
  8. customThe combined organic phase was evaporated to dryness
  9. customyielding crude product
  10. filtrationfiltered
  11. customdried to constant weight

出典と根拠

ORDレコード
ord-e41138945e2a4f5db2709c93228c4aba
出典データセット
uspto-grants-1978_01
特許番号
US04071477

関連ノート

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