Acetic Acid → Propionaldehyde 3-nitrophenylhydrazone

HRID 73922ノート

反応式

HRID 73922 の反応式
[OH-].[Na+].Cl.[N+:4]([C:7]1[CH:8]=[C:9]([NH:13][NH2:14])[CH:10]=[CH:11][CH:12]=1)([O-:6])=[O:5].C(O)(=O)C.[CH:19](=O)[CH2:20][CH3:21]>C(O)C>[N+:4]([C:7]1[CH:8]=[C:9]([NH:13][N:14]=[CH:19][CH2:20][CH3:21])[CH:10]=[CH:11][CH:12]=1)([O-:6])=[O:5]

参加物

6

反応物 4

HCID 176Acetic AcidHCID 527PropanalHCID 14798Sodium HydroxideHCID 54642853-Nitrophenylhydrazinium(1+) chloride

生成物 1

HCID 66675029Propionaldehyde 3-nitrophenylhydrazone

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Sodium hydroxide solution (10%, 15 mL) was added slowly to a stirred suspension of (3-nitro-phenyl)-hydrazine hydrochloride salt (B-4-a) (1.89 g, 10 mmol) in ethanol (20 mL) until pH 6. Acetic acid (5 mL) was added to the mixture followed by propionaldehyde (0.7 g, 12 mmol). After stirring for 3 h at room temperature, the mixture was poured into ice-water and the resulting precipitate was isolated via filtration, washed with water and dried in air to obtain N-(3-nitro-phenyl)-N′-propylidene-hydrazine, which was used directly in the next step.

後処理

  1. customthe resulting precipitate was isolated via filtration
  2. washwashed with water
  3. customdried in air

出典と根拠

ORDレコード
ord-cbed565f209f478693419be279867811
出典データセット
uspto-grants-2014_09
特許番号
US08829204B2

反応ノート

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