Diethyl Ether → 2-(3-bromobenzoyl)-N-isobutylhydrazinecarboxamide

HRID 660843

反応式

HRID 660843 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([NH:7][NH2:8])=[O:6].[CH2:12]([N:16]=[C:17]=[O:18])[CH:13]([CH3:15])[CH3:14].C(OCC)C>O1CCCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([NH:7][NH:8][C:17]([NH:16][CH2:12][CH:13]([CH3:15])[CH3:14])=[O:18])=[O:6]

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 612812-Methylpropyl isocyanateHCID 520941m-Bromobenzohydrazide

生成物 1

HCID 474281672-(3-bromobenzoyl)-N-isobutylhydrazinecarboxamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

5.00 g (23.3 mmol) of 3-bromobenzoic acid hydrazide are placed in 50 ml tetrahydrofuran at room temperature. 2.70 g (27.2 mmol) of isobutyl isocyanate, dissolved in 10 ml tetrahydrofuran, are rapidly added dropwise with stirring to this suspension. The mixture is firstly further stirred at room temperature and then allowed to stand overnight. The precipitate formed after addition of 100 ml diethyl ether is filtered off and then washed with diethyl ether. An initial quantity of 1.42 g (19% of theory) of the target compound is thus obtained. The mother liquor is concentrated, and the residue again slurried in diethyl ether and filtered. After washing with diethyl ether and drying in vacuo, a further 5.62 g (77% of theory) of the target compound remain.

後処理

  1. additionare rapidly added dropwise
  2. stirringThe mixture is firstly further stirred at room temperature
  3. customThe precipitate formed
  4. filtrationis filtered off
  5. washwashed with diethyl ether
  6. customAn initial quantity of 1.42 g (19% of theory) of the target compound is thus obtained
  7. concentrationThe mother liquor is concentrated
  8. filtrationfiltered
  9. washAfter washing with diethyl ether
  10. customdrying in vacuo

出典と根拠

ORDレコード
ord-3f37f4fe9ad4464197e67393f814bb5e
出典データセット
uspto-grants-2011_12
特許番号
US08084481B2

関連ノート

読み込み中…