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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170463Generated: November 4, 2026

Hydrochloric Acid → HCID 178478783, compound

https://huagongshe.com/reaction/1170463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178454278HCID 178454278—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 178478783HCID 178478783—

Reaction Steps

The N′,N″-di-BOC-guanidine (4a) (0.25 g, 0.4 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 (0.13 g, quantitative), mp>340° C. 1H-NMR (DMSO-d6): δ 3.95 (s, 2H), 7.24 (d, J=8.4 Hz, 2H), 7.45 (s, 2H), 7.58 (br s, 8H), 7.95 (d, J=8.4 Hz, 2H), 10.23 (br s, 2H). 13C-NMR (DMSO-d6): δ 156.1, 156.1, 144.5, 138.6, 133.8, 123.3, 121.4, 120.9, 36.8. MS (EI): m/z 277 (M++1) (14), 252 (100). Anal. Calcd. for C15H16N6.2HCl-0.25C2H5OH (364.76): C % 51.04, H % 5.39, N % 23.04, Cl % 19.44. Found: C % 50.74, H % 5.26, N % 22.99, Cl % 19.87.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825279B2
Source datasetuspto-grants-2010_11
ORD IDord-0fc11e2c7c114d0988cbd30fe353ab94
Source noteuspto-grants-2010_11