HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357130Erstellt: 25. Oktober 2026
1-Bromo-3-chloropropane → 3-benzyl-6-chloro-1-(3-chloropropyl)pyrimidine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/357130
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-benzyl-6-chloro-1H-pyrimidine-2,4-dione | HCID 937941 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-benzyl-6-chloro-1-(3-chloropropyl)pyrimidine-2,4(1H,3H)-dione | HCID 15027531 | — |
Reaktionsschritte
To a suspension of 18.93 g (80 mmol) of 3-benzyl-6-chloropyrimidine-2,4(1H,3H)-dione and 17.69 g (128 mmol) of potassium carbonate in 120 ml of N,N-dimethylformamide, 15.8 ml (160 mmol) of 1-bromo-3-chloropropane was added at room temperature. This mixture was stirred at 90° C. for 3 hours. After cooling, the reaction mixture was concentrated to dryness; the resulting residue was dissolved in chloroform-water. After the organic layer was washed with water and dried, the solvent was distilled off to yield an oily substance, which was then purified by column chromatography (eluent, n-hexane/ethyl acetate=5/1→3/1) to yield 13.46 g (53.7%, light yellow powder) of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05840732 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-6d44e8c1a720436b87fa48b2917bc808 |
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| Quellennotiz | uspto-grants-1998_11 |
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