HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357074Generated: October 26, 2026
1-Bromo-3-chloropropane → 3-benzyl-6-chloro-1-(3-chloropropyl)-5-phenylpyrimidine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/357074
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-benzyl-6-chloro-5-phenylpyrimidine-2,4(1H,3H)-dione | HCID 15027509 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-benzyl-6-chloro-1-(3-chloropropyl)-5-phenylpyrimidine-2,4(1H,3H)-dione | HCID 15027542 | — |
Reaction Steps
To a suspension of 78.19 g (250 mmol) of 3-benzyl-6-chloro-5-phenylpyrimidine-2,4(1H,3H)-dione and 55.3 g (400 mmol) of potassium carbonate in 450 ml of N,N-dimethylformamide, 49.4 ml (500 mmol) of 1-bromo-3-chloropropane was added at room temperature. This mixture was stirred at 80° C. for 5 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→2/1) to yield 71.89 g (73.9%, yellow oily substance) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840732 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-8cbc3eacec5e49abae9e5350591089e8 |
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| Source note | uspto-grants-1998_11 |
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