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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610798Generated: October 26, 2026

Hydrochloric Acid → benzyl N-[4-(azidomethyl)benzenecarboximidoyl]carbamate

https://huagongshe.com/reaction/1610798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-Amidino benzyl azideHCID 22257605—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productbenzyl N-[4-(azidomethyl)benzenecarboximidoyl]carbamateHCID 140379073—

Reaction Steps

The crystals from (ii) above were dissolved in 500 ml methylene chloride and the resulting solution was dried (K2CO3), filtered and 27 ml (194 mmol) triethyl amine was added. 25 ml Benzyl chloroformate was slowly added to the stirred solution while the reaction mixture was cooled in an ice bath. After 30 minutes an additional 2 ml benzyl chloroformate was added and stirring was continued for another 30 minutes. Subsequently, water was added and the aqueous phase was adjusted to pH 7 with 2M HCl. The organic phase was dried (MgSO4) and the solvent was removed in vacuo. 4-(benzyloxycarbonylamidino)benzyl azide was finally isolated as colorless crystals from ether/methylene chloride/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984627B1
Source datasetuspto-grants-2006_01
ORD IDord-83dd14228dc74987a3e89d1e8bfc59ba
Source noteuspto-grants-2006_01