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Urea → 5-(Butan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione

HRID 992841
ノート
印刷プレビュー

反応式

HRID 992841 の反応式
[Na].[CH:2]([CH:6]([C:11]([O:13]C)=O)[C:7]([O:9]C)=O)([CH2:4][CH3:5])[CH3:3].[NH2:15][C:16]([NH2:18])=[O:17]>C(O)C>[CH:2]([CH:6]1[C:7](=[O:9])[NH:18][C:16](=[O:17])[NH:15][C:11]1=[O:13])([CH2:4][CH3:5])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1176UreaHCID 5360545SodiumHCID 18408288Dimethyl secbutylmalonate

生成物 1

HCID 2282815-(Butan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione収率 43.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

110 mL of anhydrous ethanol was reacted with 7.72 g of sodium metal. Subsequently 17.6 g (0.1 mol) of dimethyl secbutylmalonate was added, followed (after about 5 minutes) by urea (6.72 g). The reaction mixture was refluxed for 15 hours and 60 mL of ethanol was distilled off. 200 mL of water was added to the residue followed by 20 mL of concentrated sulfuric acid. Precipitated crystals were filtered off. The product was then recrystallized from water to yield 8 g of colorless crystals.

後処理

  1. custom(after about 5 minutes)
  2. temperatureThe reaction mixture was refluxed for 15 hours
  3. distillation60 mL of ethanol was distilled off
  4. addition200 mL of water was added to the residue
  5. customPrecipitated crystals
  6. filtrationwere filtered off
  7. customThe product was then recrystallized from water

出典と根拠

ORDレコード
ord-7c3b6fcc29804eaba482e4b443da105d
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06472227B1

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート