Hydrochloric Acid → 1H-Imidazole-4-carboxaldehyde, 5-chloro-2-propyl-

HRID 2292828ノート

反応式

HRID 2292828 の反応式
[Cl:1][C:2]1[NH:6][C:5]([CH2:7][CH2:8][CH3:9])=[N:4][CH:3]=1.[CH3:10][O:11]C(N(C)C)OC.C(N(CC)CC)C.Cl.[OH-].[Na+]>ClC1C=CC=CC=1>[CH2:7]([C:5]1[NH:6][C:2]([Cl:1])=[C:3]([CH:10]=[O:11])[N:4]=1)[CH2:8][CH3:9]

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 78373Dimethylformamide dimethyl acetalHCID 21466603HCID 21466603、化合物

生成物 1

HCID 97939751H-Imidazole-4-carboxaldehyde, 5-chloro-2-propyl-

試薬・触媒・溶媒 1

HCID 7964Chlorobenzene溶媒

実験手順

A solution of 5-chloro-2-propyl-1H-imidazole (1.45 g, 10 mmol), dimethoxymethyldimethylamine (1.55 g. approximately 92 percent pure, 12 mmol) and triethylamine (0.10 g, 1 mmol) in chlorobenzene (50 ml) was heated for 1 hour at 80% and 2.5 hours under reflux, cooled to room temperature and poured into 2M hydrochloric acid (100 ml). The pH was adjusted to pH 1.97 by addition of 30 percent strength sodium hydroxide solution (19 ml) and the mixture was extracted three times, each time with 50 ml of ethyl acetate. The combined organic phases were dried and concentrated on a rotavapor. The yield of the product was 1.27 g (approximately 90 percent pure according to H-NMR), 66 percent based on 5-chloro-2-propyl-1H-imidazole. Other data concerning the product was:

後処理

  1. temperatureunder reflux
  2. extractionthe mixture was extracted three times
  3. customThe combined organic phases were dried
  4. concentrationconcentrated on a rotavapor

出典と根拠

ORDレコード
ord-a05b149d9b974d9c941b2a1d399aa19c
出典データセット
uspto-grants-1997_11
特許番号
US05684157

反応ノート

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