Benzaldehyde → N'-benzylidene-4-trifluoromethylbenzohydrazide

HRID 1354412ノート

反応式

HRID 1354412 の反応式
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:12]=[CH:11][C:6]([C:7]([NH:9][NH2:10])=[O:8])=[CH:5][CH:4]=1.[CH:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.S(=O)(=O)(O)O>CO>[CH:15](=[N:10][NH:9][C:7](=[O:8])[C:6]1[CH:11]=[CH:12][C:3]([C:2]([F:13])([F:14])[F:1])=[CH:4][CH:5]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

5

反応物 3

HCID 240BenzaldehydeHCID 1118Sulfuric AcidHCID 5206624-(Trifluoromethyl)benzohydrazide

生成物 1

HCID 6736306N'-benzylidene-4-trifluoromethylbenzohydrazide収率 74%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution (50 ml) of 4-trifluoromethylbenzohydrazide (3.06 g) and benzaldehyde (1.52 ml) in methanol was added dropwise conc. sulfuric acid (0.5 ml), and this mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated, and the residue was washed with hexane-ethanol (1:1, volume ratio) and recrystallized from ethanol to give N′-benzylidene-4-trifluoromethylbenzohydrazide (3.23 g, yield 74%) as colorless needle crystals. melting point: 216–217° C.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. washthe residue was washed with hexane-ethanol (1:1, volume ratio)
  3. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-04360be69d8a45b491ff0ea21c329994
出典データセット
uspto-grants-2007_05
特許番号
US07223791B2

反応ノート

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