HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597722Generated: October 25, 2026
Hydrochloric Acid → HCID 178465768, compound
https://huagongshe.com/reaction/597722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,5-Dibromo-2-ethoxybenzaldehyde | HCID 291807 | — |
| Reactant | HCID 178479531 | HCID 178479531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178465768 | HCID 178465768 | — |
Reaction Steps
A mixture was prepared by dissolving 7.9 grams (0.063 mole) of diaminoguanidine, hydrochloride in 60 milliliters of lukewarm water and this mixture was added to a solution of 38.2 grams (0.125 mole) of 3,5-dibromo-2-ethoxybenzaldehyde dissolved in 500 milliliters of ethanol. To this mixture was added a solution of 8 milliliters of concentrated hydrochloric acid in 80 milliliters of ethanol. The mixture was heated at the reflux temperature for 10 minutes and thereafter cooled to 20° C. The solid 1,3-bis[(3,5-dibromo-2-ethoxybenzylidene)amino]guanidine, hydrochloride product was recovered by filtration under reduced pressure, washed with ethanol and dried. The product was recovered in a yield of 20 grams (45 percent of theoretical) and melted at 188°-190° C.
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-197343b44ee34a44be2b84f2790b3ac4 |
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| Source note | uspto-grants-1977_03 |
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