Diethyl Sulfate → HCID 178467037、化合物

HRID 1579247ノート

反応式

HRID 1579247 の反応式
[CH3:1][O:2][C:3]1[N:8]=[C:7]([OH:9])[CH:6]=[C:5]([OH:10])[N:4]=1.S(OCC)(O[CH2:15][CH3:16])(=O)=O>[OH-].[Na+]>[CH3:1][O:2][C:3]1[N:8]=[C:7]([O:9][CH2:15][CH3:16])[CH:6]=[C:5]([OH:10])[N:4]=1

参加物

4

反応物 2

HCID 6163Diethyl SulfateHCID 178494256HCID 178494256、化合物

生成物 1

HCID 178467037HCID 178467037、化合物

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒3 回

実験手順

14.2 g (0.1 mol) of 2-methoxy-4,6-dihydroxypyrimidine are added while stirring to 50 cc of 2N sodium hydroxide solution 2N and the mixture is stirred for half an hour with heating to 50°. 17.0 g (0.11 mol) of diethyl sulphate are subsequently added dropwise, over the course of 20 minutes and with stirring; by adding 2N sodium hydroxide solution the pH value should, if possible, be kept at between 8 and 8.2. The mixture is then stirred at 50°, 2N sodium hydroxide solution is added from time to time until the pH remains constant (after approximately 3 hours). The reaction mixture is subsequently cooled to 0°, the precipitate is suction filtered and washed with a small quantity of ethanol. After drying in a high vacuum at 80°, the substance has a M.P. of 192°-194°.

後処理

  1. temperaturewith heating to 50°
  2. stirringwith stirring
  3. stirringThe mixture is then stirred at 50°
  4. custom(after approximately 3 hours)
  5. temperatureThe reaction mixture is subsequently cooled to 0°
  6. filtrationfiltered
  7. washwashed with a small quantity of ethanol
  8. customAfter drying in a high vacuum at 80°

出典と根拠

ORDレコード
ord-1686a36b50bb4628a85cb2b50e265417
出典データセット
uspto-grants-1976_01
特許番号
US03931180

反応ノート

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