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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422124Generated: October 29, 2026

Hydrochloric Acid → Bis-guanidine dihydrochloride

https://huagongshe.com/reaction/422124

Reaction equation

Participants

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

Reaction Steps

The N′,N″-di-BOCguanidine (0.45 g, 0.60 mmol) was dissolvedin 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 numberUS08101636B2
Source datasetuspto-grants-2012_01
ORD IDord-58621fac3ff84331a967aac9e86f46fb
Source noteuspto-grants-2012_01