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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Benzyloxy)-3,5-dibromobenzaldehyde | HCID 1494337 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178479531 | HCID 178479531 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 178512744 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04015016 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-fde0dd452c434535aee026afdb908733 |
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| Source note | uspto-grants-1977_03 |
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