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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862952Generated: October 25, 2026

Allyl chloride → 1,3-Diallyl-5,5-dimethylhydantoin

https://huagongshe.com/reaction/1862952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSodium hydrideHCID 24758—
Reactant3-Allyl-5,5-dimethylhydantoinHCID 597696—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,3-Diallyl-5,5-dimethylhydantoinHCID 920029—

Reaction Steps

To a slurry of 4.8 grams (0.1 mole) of a 50% sodium hydride mineral oil dispersion in 35 ml. of DMF was added portionwise with stirring 17.6 grams (0.105 mole) of 3-allyl-5,5-dimethylhydantoin. Hydrogen was evolved in this exothermic reaction. The reaction mixture was heated and stirred at 55°-60° C. for 1 hour till the gas evolution ceased and a clear solution resulted. To the solution was added dropwise with stirring over a 10-minute period keeping the temperature below 80° C. 9.3 grams (0.12 mole) of allyl chloride. The reaction mixture was then heated at 55°-60° C. for 1.5 hours. Following cooling to room temperature, the reaction mixture was poured into 100 ml of water. An oily product was formed which was extracted using benzene and purified by vacuum distillation. The above named product was obtained in a yield of 14.15 grams (68%) boiling at 89°-92° C./0.1 mm. (Compound 3)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167465
Source datasetuspto-grants-1979_09
ORD IDord-4bf0f6d9855a4f14a9d4d0f5c390f321
Source noteuspto-grants-1979_09