HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420849Generated: October 29, 2026
Hydrochloric Acid → HCID 60887576, compound
https://huagongshe.com/reaction/420849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 3-Hydroxyacetophenone | HCID 8487 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 60887576 | HCID 60887576 | — |
Reaction Steps
3′-Hydroxyacetophenone (1.0 g) and ethylenediamine (1.47 ml) were dissolved in methanol (10 ml), and the solution was stirred at room temperature for 16 hours. The mixture was added with sodium borohydride (277.9 mg), and the mixture was stirred at room temperature for 5 hours. The reaction mixture was added with 1 N hydrochloric acid, and then the solvent was evaporated. The residue was added with potassium carbonate and distilled water, thereby made alkaline, and then extracted with a mixed solvent of chloroform-ethanol (10:1), and the organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol:28% aqueous ammonia=10:1:0.1 to 5:1:0.1) to obtain the title compound (59.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097708B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b0c9900a7ea142288d4c088febfbd87f |
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| Source note | uspto-grants-2012_01 |
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