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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973912Generated: November 1, 2026

Chlorosuccinimide → HCID 19987104, compound

https://huagongshe.com/reaction/973912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 19987105HCID 19987105—
SolventAcetonitrileHCID 6342—
ProductHCID 19987104HCID 19987104111.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution containing 20 g of 6-chloro-3-(2-ethylhexyl)-1-methyluracil thus-obtained in 50 ml of acetonitrile was added 8.6 g of N-chlorosuccinimide, the mixture was heated to 40° C. and stirred for 2 hours. After allowing the mixture to cool, the acetonitrile was distilled off under reduced pressure, to the residue was added water and it was extracted with 100 ml of chloroform. The organic phase was washed with a saturated aqueous sodium chloride solution and dried with anhydrous magnesium sulfate. The chloroform was distilled off under reduced pressure, and the residue was purified by silica gel chromatography to obtain 22 g of 5,6-dichloro-3-(2-ethylhexyl)-1-methyluracil as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066573
Source datasetuspto-grants-1991_11
ORD IDord-f593d09ffeea4c11ad906ff919de8352
Source noteuspto-grants-1991_11