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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609561Generated: October 31, 2026

Sodium Carbonate → HCID 178479315, compound

https://huagongshe.com/reaction/609561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Chlorobenzoyl chlorideHCID 69110—
ReactantHCID 178478772HCID 178478772—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178479315HCID 178479315—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the product of Example 1, step (b), 1.38 g, 0.0050 moles, was dissolved in 20 ml of water. The solution was gradually treated with sodium carbonate, 0.84 g, 0.0100 moles, and cooled to 0° C. A solution of 2-chlorobenzoyl chloride, 0.96 g, 0.0053 moles, in 10 ml of tetrahydrofuran was added. This mixture was allowed to stir over the weekend. The mixture was then diluted with water to 100 ml and washed with 20 ml of chloroform. The mixture was made basic with 50% sodium hydroxide and extracted with 20 ml of chloroform (twice). The chloroform was dried with potassium carbonate, filtered and evaporated by vacuum evaporation. The residue was taken up in 20 ml of isopropanol, treated with 1 ml of concentrated hydrochloric acid, and then diluted to 250 ml with ether. The solid that precipitated was collected by filtration and washed with 10 ml of ether (twice). The solid was then recrystallized with methanol and ether and dried in the vacuum oven to provide N-(3-(((2-chlorophenyl)carbonyl)amino)phenyl)-1-pyrrolidinecarboximidamide monohydrochloride. Yield: 1.1 g, m.p. 145° C. (dec)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998399
Source datasetuspto-grants-1999_12
ORD IDord-a707990392e9443abfe5927934d064db
Source noteuspto-grants-1999_12