HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357116Generated: October 25, 2026
1-Bromo-3-chloropropane → 6-chloro-1-(3-chloropropyl)-3,5-dibenzylpyrimidine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/357116
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-chloro-3,5-dibenzylpyrimidine-2,4(1H,3H)-dione | HCID 18936661 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-chloro-1-(3-chloropropyl)-3,5-dibenzylpyrimidine-2,4(1H,3H)-dione | HCID 18936861 | — |
Reaction Steps
To a suspension of 24.51 g (75 mmol) of 6-chloro-3,5-dibenzylpyrimidine-2,4(1H,3H)-dione and 16.58 g (120 mmol) of potassium carbonate in 120 ml of N,N-dimethylformamide, 14.8 ml (150 mmol) of 1-bromo-3-chloropropane was added at room temperature. This mixture was stirred at 90° C. for 2 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 22.68 g (74.9%, 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-93fa0b5c96694328966cfd43a9eefa0f |
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| Source note | uspto-grants-1998_11 |
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