HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876096Generated: October 30, 2026
Ethylenediamine → HCID 17854996, compound
https://huagongshe.com/reaction/876096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-Vinylbenzyl chloride | HCID 74126 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 17854996 | HCID 17854996 | 11.6% |
Reaction Steps
In a 500 mL, 3-necked round-bottomed flask were taken 5.31 grams of 1,2-ethylenediamine and 32.48 g of anhydrous potassium carbonate, and 300 mL of chloroform. To this suspension was added 30 g of 4-vinylbenzyl chloride. The resulting reaction mixture was stirred at 25° C. for 18 hr. Subsequently the reaction mixture was filtered. The solvent was moved under reduced pressure. To the residue was added 300 mL of deionized water followed by 37% aqueous HCl until the pH of the solution was 2.0. The resulting aqueous solution was extracted with tert-butyl methyl ether (2×250 mL). The aqueous layer was collected and was treated with 40% (w/w) NaOH until the pH of the solution was 11.4. The resulting aqueous solution was extracted with tert-butyl methyl ether (2×250 mL). The organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was removed under reduced pressure yielding 3 g of the product as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08986669B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-c99bb742d82c4fa084501594d7827062 |
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| Source note | uspto-grants-2015_03 |
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