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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930500Generated: November 2, 2026

Hydrochloric Acid → Bis-guanidine dihydrochloride

https://huagongshe.com/reaction/1930500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N'-Di-Boc-guanidineHCID 4124838—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductBis-guanidine dihydrochlorideHCID 73947521—

Reaction Steps

The N′,N″-di-BOCguanidine (0.45 g, 0.60 mmol) was dissolved in CH2Cl2 (10 mL), diluted with dry EtOH (15 mL) and the chilled solution was saturated with dry HCl. The reaction was then kept stirring at room temperature for 3 days (drying tube), when by the product started forming a precipitate over time. After evaporating the solvent to dryness, the residue was washed with ether multiple times and was dried under vacuum at 50-60° C. over night to give whitish yellow solid of the bis-guanidine dihydrochloride; mp >300° C. 1H NMR (DMSO-d6): δ 7.85 (dd, J=1.5, 8.4 Hz, 4H), 7.92 (d, J=1.2 Hz, 4H), 8.00 (dd, J=1.5, 8.4 Hz, 4H), 9.09 (br s, 4H), 11.25 (br s, 2H). 13C NMR (DMSO-d6): δ 155.98, 138.35, 137.32, 135.00, 127.79, 127.22, 124.79. MS (ESI) m/e (rel. int.): 344 (M+, 6), 173 (100). Anal. Calc. for C20H20N6-2.0HCl-1.0H2O-0.2C2H5OH: C %, 55.11; H %, 5.71; N %, 18.90. Found C %, 55.39; H %, 5.50; N %, 18.71.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188121B2
Source datasetuspto-grants-2012_05
ORD IDord-71bc1b617ff14339b179d14c44294850
Source noteuspto-grants-2012_05