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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812402Generated: October 30, 2026

Dichloromethane → N-isopropyl-N-methyl-1H-imidazole-1-carboxamide

https://huagongshe.com/reaction/1812402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ProductN-isopropyl-N-methyl-1H-imidazole-1-carboxamideHCID 6661111580%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 50 mL round-bottomed flask was added 1,1′-carbonyldiimidazole (1.663 g, 10.25 mmol), (Fluka Chemie) DCM (25 mL). The solution was stirred at 0° C. using a water bath and treated in one portion with n-isopropylmethylamine (0.5 mL, 6.84 mmol) (Aldrich). The water bath was removed, and the solution was stirred at room temperature. After 2 hours all starting material was consumed. The reaction mixture was diluted with DCM (10 mL) and quenched with water. The organic layer was separated, dried over sodium sulfate and concentrated to afford N-isopropyl-N-methyl-1H-imidazole-1-carboxamide (0.920 g, 5.50 mmol, 80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-efc067954ef04f51b203211d9125d83d
Source noteuspto-grants-2013_01