HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1580125Erstellt: 26. Oktober 2026
Hydrochloric Acid → 1-(2-Hydroxy-5-nitrobenzyl)-2-imidazolidinone
https://huagongshe.com/reaction/1580125
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | 2-Imidazolidinone | HCID 8453 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Hydroxy-5-nitrobenzyl bromide | HCID 13044 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(2-Hydroxy-5-nitrobenzyl)-2-imidazolidinone | HCID 13006892 | — |
Reaktionsschritte
A 7.9 g (0.092 mole) portion of 2-imidazolidinone in 92 ml of dimethylsulfoxide was treated with 12.7 g (0.092 mole) of K2CO3, 7.4 g (0.045 mole) of potassium iodide and 20.0 g (0.092 mole) of 2-hydroxy-5-nitrobenzyl bromide. The reaction mixture was heated to 105° over 0.3 hours and held at 105° for 1.6 hours. The reaction mixture was poured with stirring into 550 ml of water. The aqueous mixture was acidified with 9 ml of concentrated HCl and extracted with 480 ml of chloroform. The chloroform extract was washed with 60 ml of H2O, dried over MgSO4 overnight and filtered. The filtrate was concentrated under reduced pressure to give 18 g of a yellow semi-solid. The crude product was crystallized using 65 ml of benzene and filtered, washing with ether to give 9.7 g (44%) of a light yellow semi-solid. Recrystallization from acetonitrile gave an analytical sample, m.p. 222°-224° dec.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03932452 |
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| Quelldatensatz | uspto-grants-1976_01 |
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| ORD ID | ord-68b133b975dd448389ab1c8fc39c6058 |
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| Quellennotiz | uspto-grants-1976_01 |
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