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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844481Generated: October 29, 2026

Guanidine Hydrochloride → HCID 178513108, compound

https://huagongshe.com/reaction/844481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
SolventWaterHCID 962—
ProductHCID 178513108HCID 178513108—

Reaction Conditions

Temperature0 °C

Reaction Steps

1,4-Dioxane (20 ml) is added to a solution of guanidine hydrochloride (0.96 g, 10 mmol) and sodium hydroxide (0.8 g, 20 mmol) in water (10 ml) and the resulting mixture is cooled to 0° C. Benzyloxycarbonyl chloride (1.1 ml, 7.7 mmol) is added dropwise with vigorous stirring over a period of 10 min. After the addition is completed, the ice-bath is removed and stirring is continued for 1 h at room temperature. The mixture is concentrated in vacuo to one third of its original volume and extracted three times with ethyl acetate (20 ml each). The combined extracts are washed with brine (20 ml) and dried with anhydrous sodium sulfate. After filtering and removal of the solvent under reduced pressure N-Cbz-guanidine (1.31 g, 88%) is obtained as a white powder: mp: 120-122° C.; 1H NMR (360 MHz, DMSO-d6) δ 7.35-7.25 (m, 5H), 6.88 (br s, 4H), 4.95 (s, 2H); Electrospray-MS m/e 194 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380358B1
Source datasetuspto-grants-2002_04
ORD IDord-70be4355e83a4321a7c443f27944441d
Source noteuspto-grants-2002_04