Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184673Generated: October 27, 2026

Guanidine Hydrochloride → HCID 178513094, compound

https://huagongshe.com/reaction/1184673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2,3-Methylenedioxycinnamic acidHCID 4451078—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
ProductHCID 178513094HCID 17851309466%

Reaction Steps

Oxalyl chloride (0.68 mL, 7.8 mmol) was added to a suspension of 2,3-methylenedioxycinnamic acid (500 mg, 2.6 mmol) in dichloromethane (5 nm) containing a drop of dimethylformamide. The mixture was stirred for 25 hours and the resulting solution was evaporated to dryness under reduced pressure. The residue was dissolved in dry tetrahydrofuran (5 mL) and added to a solution of guanidine hydrochloride (1.24 g, 13 mmol) in 2M aqueous sodium hydroxide (8 mL). The reaction was stirred at room temperature for 1 hour and chloroform was then added. The resulting precipitate of crude product (100 mg) was collected by filtration. The filtrate was extracted with chloroform (3×30 mL) and ethyl acetate (20 mL). The combined organic extracts were washed with 2M aqueous sodium hydroxide (20 mL), water (20 mL), dried (Na2SO4) and concentrated under reduced pressure to give a further quantity of crude product (400 mg). The two crops of crude product were combined, suspended in chloroform (10 mL) and stirred vigorously for 20 minutes. The resulting 2,3-methylenedioxycinnamoylguanidine (420 mg) was collected by filtration and dried under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669280B2
Source datasetuspto-grants-2014_03
ORD IDord-708d1415cd2a495893ec6c3dc5c877ac
Source noteuspto-grants-2014_03