ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

DL-norvaline → HCID 178440053、化合物

HRID 1462217
ノート
印刷プレビュー

反応式

HRID 1462217 の反応式
[N:1](=[C:3]([C:7](=[O:9])[CH3:8])[C:4](=O)[CH3:5])O.[NH2:10][CH:11](C(O)=O)[CH2:12][CH2:13][CH3:14]>C(#N)C>[C:7]([C:3]1[NH:1][C:11]([CH2:12][CH2:13][CH3:14])=[N:10][C:4]=1[CH3:5])(=[O:9])[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 824DL-norvalineHCID 178468373HCID 178468373、化合物

生成物 1

HCID 178440053HCID 178440053、化合物収率 43.5%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

An acetonitrile (250 ml) mixture of 3-oximino-2, 4-pentanedione (40 g, 0.31 moles) and d,1-norvaline (43.55 g, 0.372 moles) was heated to reflux under nitrogen. After 23.7 h the reaction mixture was allowed to cool, then suction filtered. The residue was washed with acetonitrile and the combined filtrates concentrated in vacuo. After dissolving the resulting oil in ethyl acetate (100 ml), it was washed with three 40 ml portions of 5% aqueous sodium hydroxide solution. The combined organic extracts were dried over anhydrous potassium carbonate and then concentrated in vacuo to give 0.1 moles (43.5% yield based on recovered d,1-norvaline) of 5-acetyl-4-methyl-2-propylimidazole.

後処理

  1. temperaturewas heated
  2. temperatureto reflux under nitrogen
  3. temperatureto cool
  4. filtrationsuction filtered
  5. washThe residue was washed with acetonitrile
  6. concentrationthe combined filtrates concentrated in vacuo
  7. dissolutionAfter dissolving the resulting oil in ethyl acetate (100 ml)
  8. washit was washed with three 40 ml portions of 5% aqueous sodium hydroxide solution
  9. dry with materialThe combined organic extracts were dried over anhydrous potassium carbonate
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-babd9dfe7a424fbba1d709db82730dd4
出典データセット
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04459413

反応ノート

読み込み中…

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