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Hydrochloric Acid → HCID 178437660、化合物

HRID 1828825
ノート
印刷プレビュー

反応式

HRID 1828825 の反応式
Br[C:2]1[N:3]=[C:4]([CH2:12][CH3:13])[N:5](COC)[C:6]=1[CH:7]=[O:8].[ClH:14]>>[Cl:14][C:2]1[N:3]=[C:4]([CH2:12][CH3:13])[NH:5][C:6]=1[CH:7]=[O:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 313Hydrochloric AcidHCID 220585604-Bromo-2-ethyl-1-(methoxymethyl)imidazole-5-carbaldehyde

生成物 1

HCID 178437660HCID 178437660、化合物

反応条件

温度
90 °C

実験手順

4-Bromo-2-ethyl-1-(methoxymethyl)imidazole-5-carbaldehyde (365 g) was dissolved in 35% conc. hydrochloric acid (1.8 L), and the mixture was heated at 90° C. for 20 hr. The solvent was evaporated under reduced pressure, and sodium hydrogencarbonate was added to the residue under ice-cooling until the mixture assumed weak alkalinity. The mixture was extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and diisopropyl ether was added to the residue. The mixture was heated and allowed to cool. The precipitated crystals were collected by filtration and dried by heating under reduced pressure to give 4-chloro-2-ethylimidazole-5-carbaldehyde (211.5 g) as brown crystals.

後処理

  1. customThe solvent was evaporated under reduced pressure, and sodium hydrogencarbonate
  2. additionwas added to the residue under ice-
  3. temperaturecooling until the mixture
  4. extractionThe mixture was extracted with chloroform
  5. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure and diisopropyl ether
  7. additionwas added to the residue
  8. temperatureThe mixture was heated
  9. temperatureto cool
  10. filtrationThe precipitated crystals were collected by filtration
  11. customdried
  12. temperatureby heating under reduced pressure

出典と根拠

ORDレコード
ord-e8fcc67d339e4df6a7e92c0b50ea4eae
出典データセット
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07060721B1

反応ノート

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