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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597721Generated: October 25, 2026

2-(Benzyloxy)-3,5-dibromobenzaldehyde → HCID 178512744, compound

https://huagongshe.com/reaction/597721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy)-3,5-dibromobenzaldehydeHCID 1494337—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178479531HCID 178479531—
SolventHydrochloric AcidHCID 313—
ProductHCID 178512744HCID 178512744—

Reaction Steps

To a mixture of 2.1 grams (0.015 mole) of N,N'-diaminoguanidine, hydrochloride in 50 milliliters of 2B-ethanol and 2.0 milliliters of concentrated hydrochloric acid was added 11.1 grams (0.03 mole) of 2-benzyloxy-3,5-dibromobenzaldehyde. The mixture was stirred and heated to reflux temperature and maintained at this temperature overnight. At the completion of the reaction, the insoluble crystals contained in the reaction mixture were removed by filtration and dried under reduced pressure. The solid crude 1,3-bis[((3,5-dibromo-2-benzyloxybenzylidene)-amino]guanidine, hydrochloride product was mixed with 250 milliliters of benzene refluxed, recovered by filtration and dried. The product was obtained in a yield of 11.3 grams and melted at 217°-218° C. Upon analysis, the product was found to have carbon, hydrogen and nitrogen contents of 41.83, 3.00 and 8.48 percent, respectively, as compared with the theoretical contents of 41.98, 2.92 and 8.44 percent, respectively, calculated for the abovenamed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04015016
Source datasetuspto-grants-1977_03
ORD IDord-fde0dd452c434535aee026afdb908733
Source noteuspto-grants-1977_03