HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459416Generated: October 30, 2026
Bromine → 6-(1-Bromoethyl)-2,4-dichloro-5-fluoropyrimidine
https://huagongshe.com/reaction/459416
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,4-Dichloro-6-ethyl-5-fluoropyrimidine | HCID 22323353 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(1-Bromoethyl)-2,4-dichloro-5-fluoropyrimidine | HCID 22323339 | 95% |
Reaction Steps
A mixture of the compound of part (i) (400 g), N-bromosuccinimide (730 g), azoisobutyronitrile (33.7 g), bromine (65.5 g) and water (6.4 L) was heated at 80–85° C. for 5 hours. Further N-bromosuccinimide (183 g) was added, heating continued for 2 hours then further azoisobutyronitrile (33.7 g) added. After heating for 2 hours at 85° C. further azoisobutyronitrile (33.7 g) was added and heating continued for 3 hours. The reaction was cooled, diluted with water (4 L) and extracted with dichloromethane (2×3 L). The combined organic extracts were washed with a solution of sodium metabisulphate (600 g) in water (2.5 L), followed by water (3 L). The solvent was removed by evaporation under reduced pressure, toluene (1.0 L) added and the solution concentrated under reduced pressure to give the product as an oil (534 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07193083B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-fca3c9b202584e859da42c5504b3bb1d |
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| Source note | uspto-grants-2007_03 |
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