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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantN-bromobutanimideHCID 67184—
Reactant2,4-Dichloro-6-ethyl-5-fluoropyrimidineHCID 22323353—
SolventWaterHCID 962—
Product6-(1-Bromoethyl)-2,4-dichloro-5-fluoropyrimidineHCID 2232333995%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07193083B2
Source datasetuspto-grants-2007_03
ORD IDord-fca3c9b202584e859da42c5504b3bb1d
Source noteuspto-grants-2007_03