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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735502Generated: October 25, 2026

Sodium Hydroxide → 2-Butyl-5-chloro-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/1735502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 136375570—
SolventWaterHCID 962—
Product2-Butyl-5-chloro-1H-imidazole-4-carbaldehydeHCID 5517693%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1.00 g (5.12 mmol) of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one and 3.20 g (20.48 mmol) of POCl3 was heated at 100° C. for 45 minutes. Then, 1.76 g of POCl3 was distilled off on the Rotavapor, and the residue was treated with 6 ml of ethyl acetate. The mixture thus obtained was added to 20 ml of water, and the water was stirred at room temperature for 5 minutes. Then, the pH was adjusted from 0.34 to 7, using 30 percent strength sodium hydroxide solution. The mixture was extracted twice, using 10 ml of ethyl acetate each time. The combined organic phases were dried (MgSO4), filtered and concentrated, and the residue was dried in a high vacuum. 0.89 g of 2-butyl-5-chloroimidazole-4-carbaldehyde was obtained; this product having a purity greater than 95 percent, according to H-NMR. This corresponds to a yield of 93 percent, based on the 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536841
Source datasetuspto-grants-1996_07
ORD IDord-79c53c5c85284213b9b85729a56bf8d2
Source noteuspto-grants-1996_07