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Nitric Acid → 2,5-Dimethyl-1H-imidazole-4-carbaldehyde

HRID 1413255
ノート
印刷プレビュー

反応式

HRID 1413255 の反応式
[CH3:1][C:2]1[NH:3][C:4]([CH3:9])=[C:5]([CH2:7][OH:8])[N:6]=1.[N+]([O-])(O)=O.C(=O)([O-])[O-].[Na+].[Na+]>>[CH3:1][C:2]1[NH:3][C:4]([CH3:9])=[C:5]([CH:7]=[O:8])[N:6]=1
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 3

HCID 944Nitric AcidHCID 10340Sodium CarbonateHCID 12647302HCID 12647302、化合物

生成物 1

HCID 132064322,5-Dimethyl-1H-imidazole-4-carbaldehyde

実験手順

A 42.2 gm. portion of 2,5-dimethyl-4-imidazolemethanol and 44.8 ml. of concentrated nitric acid are mixed. When the initial reaction subsides, the solution is heated on a steam bath for 1 hour. The reaction mixture is neutralized with concentrated aqueous sodium carbonate, then concentrated under vacuum. After leaching the residue with 150 ml. of hot ethanol several times, the combined organic solution are concentrated under vacuum. Chromatographing the residual oil on silica gel gives a solid which is recrystallized from isopropanolethyl acetate to give the desired product, m.p. 164.5°-166° C.

後処理

  1. customWhen the initial reaction subsides
  2. temperaturethe solution is heated on a steam bath for 1 hour
  3. concentrationconcentrated under vacuum
  4. concentrationof hot ethanol several times, the combined organic solution are concentrated under vacuum
  5. customChromatographing the residual oil on silica gel gives a solid which
  6. customis recrystallized from isopropanolethyl acetate

出典と根拠

ORDレコード
ord-e16a3fc35f684cdbac26f2115bd316c9
出典データセット
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE030511

反応ノート

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