HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940221Generated: October 31, 2026
Hydrochloric Acid → 1H-Imidazole-4-carboxaldehyde, 5-chloro-2-propyl-
https://huagongshe.com/reaction/1940221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 21466603 | HCID 21466603 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1H-Imidazole-4-carboxaldehyde, 5-chloro-2-propyl- | HCID 9793975 | — |
Reaction Steps
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° C. 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:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698707 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-ad3d25c0447c40c393d9c4fb1465d50e |
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| Source note | uspto-grants-1997_12 |
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