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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459411Generated: October 31, 2026

Iodine → 2,4-Dichloro-6-ethyl-5-fluoropyrimidine

https://huagongshe.com/reaction/459411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl BromideHCID 6332—
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventTriethylamineHCID 8471—
Product2,4-Dichloro-6-ethyl-5-fluoropyrimidineHCID 2232335376.4%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a stirred mixture of magnesium turnings (12.1 kg) in tetrahydrofuran (161 L) was added a solution of bromoethane (54.3 kg) in tetrahydrofuran (53 L) maintaining the reaction temperature below 50° C. during the addition. The solution of the Grignard reagent was cooled to 0° C. and a solution of the compound of part (i) (56 kg) in dimethoxyethane (170 L) added, maintaining the reaction temperature below 15° C. during the addition. The reaction was stirred for 1 hour at 15° C. and cooled to 0° C. A solution of triethylamine (34 kg) in tetrahydrofuran (70 L) was added, maintaining the reaction temperature at about 5° C., followed by a solution of iodine (85 kg) in tetrahydrofuran (256 L), maintaining the reaction temperature below 15° C. The reaction was then quenched with water (840 L), maintaining the reaction temperature below 25° C. The pH was adjusted to 1 using 5N aqueous hydrochloric acid solution (50 L) and the mixture extracted with toluene (1×490 L followed by 1×210 L). The combined organic layers were washed with 2% w/w aqueous sodium metabisulphite solution (700 L) then water (700 L) added and the remaining tetrahydrofuran removed by distillation under reduced pressure. The mixture was cooled, the organic layer separated, washed with water (425 L) and then concentrated under reduced pressure to provide the product as an oil (50 kg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07193083B2
Source datasetuspto-grants-2007_03
ORD IDord-c04eb0237dfe43cca6d2030a0be14512
Source noteuspto-grants-2007_03