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Theobromine → HCID 20041114、化合物

HRID 1762551
ノート
印刷プレビュー

反応式

HRID 1762551 の反応式
[CH3:1][N:2]1[C:10]2[N:9]=[CH:8][N:7]([CH3:11])[C:6]=2[C:5](=[O:12])[NH:4][C:3]1=[O:13].Cl[CH2:15][CH2:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:1][N:2]1[C:10]2[N:9]=[CH:8][N:7]([CH3:11])[C:6]=2[C:5](=[O:12])[N:4]([CH2:15][CH2:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])[C:3]1=[O:13]
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 5429TheobromineHCID 11430Potassium CarbonateHCID 133573926-Chloro-2-methylhex-2-ene

生成物 1

HCID 20041114HCID 20041114、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

9.0 g (0.05 mol) of 3,7-dimethylxanthine, 8.0 g (0.06 mol) of 1-chloro-5-methyl-4-hexene and 8.3 g (0.06 mol) of potassium carbonate are stirred in 200 ml of dimethylformamide at 110° C. for 22 hours. After the solvent has been removed in vacuo, 100 ml of 1N sodium hydroxide solution are added and the mixture is extracted thoroughly with methylene chloride. The extract is extracted again by shaking with dilute sodium hydroxide solution, washed with water until neutral, dried and evaporated under reduced pressure and the residue is recrystallized from diisopropyl ether.

後処理

  1. customAfter the solvent has been removed in vacuo, 100 ml of 1N sodium hydroxide solution
  2. additionare added
  3. extractionthe mixture is extracted thoroughly with methylene chloride
  4. extractionThe extract is extracted again
  5. washwashed with water until neutral,
  6. customdried
  7. customevaporated under reduced pressure
  8. customthe residue is recrystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-52f373a3bdbb44d9b9796d537f485edf
出典データセット
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04833146

反応ノート

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