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Urea → 5-(1-Methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione

HRID 1643354
ノート
印刷プレビュー

反応式

HRID 1643354 の反応式
[Na].[C:2]([O:10]CC)(=O)[CH2:3][C:4]([O:6]CC)=O.Br[CH:14]([CH3:16])[CH3:15].[NH2:17][C:18]([NH2:20])=[O:19]>C(O)C.CO.O.Cl>[CH:14]([CH:3]1[C:2](=[O:10])[NH:20][C:18](=[O:19])[NH:17][C:4]1=[O:6])([CH3:16])[CH3:15]
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

9

反応物 4

HCID 1176UreaHCID 63582-BromopropaneHCID 7761Diethyl MalonateHCID 5360545Sodium2 回

生成物 1

HCID 818745-(1-Methylethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione収率 43.4%

試薬・触媒・溶媒 4

HCID 313Hydrochloric Acid溶媒
HCID 702
Ethanol
溶媒
HCID 887Methanol溶媒
HCID 962Water溶媒

反応条件

温度
80 °C

実験手順

Sodium metal (1.28 kg, 55.65 mol) was dissolved in ethanol (25 L) under nitrogen atmosphere at 0° C. (bath temperature). Diethyl malonate (7.45 kg, 46.51 mol) was added to the solution and the mixture was heated to 80° C. 2-Bromopropane (8.00 kg, 65 mol) was added dropwise to the solution for 1 hour, and the solution was refluxed for 10 hours. The solution was cooled to room temperature. Sodium metal (1.22 kg, 53.04 mol) was dissolved into the solution under nitrogen atmosphere at 0° C. Urea (2.78 kg, 46.28 mol) in methanol (15 L) was added to the solution over 2 hours and the reaction mixture was refluxed for 20 hours. The reaction mixture was diluted with water (35 L) and conc. HCl (5 L), and cooled to room temperature. The precipitate was collected by filtration, washed with water (20 L), ether (15 L), n-hexane (20 L) and dried in vacuum at 40° C. for 10 hours to give 5-isopropylbarbituric acid as a white solid (3.42 kg, 20.10 mol, 43% yield).

後処理

  1. temperaturethe solution was refluxed for 10 hours
  2. temperatureThe solution was cooled to room temperature
  3. temperaturethe reaction mixture was refluxed for 20 hours
  4. temperaturecooled to room temperature
  5. filtrationThe precipitate was collected by filtration
  6. washwashed with water (20 L), ether (15 L), n-hexane (20 L)
  7. customdried in vacuum at 40° C. for 10 hours

出典と根拠

ORDレコード
ord-c6053edb77fd44cabe31e4607f917f38
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08119800B2

反応ノート

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