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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166678Generated: November 4, 2026

1,3-Dibromo-5,5-dimethylhydantoin → HCID 53799402, compound

https://huagongshe.com/reaction/2166678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantHCID 54235062HCID 54235062—
SolventO-XyleneHCID 7237—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 53799402HCID 5379940292.8%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 1α,3β-dimethoxycarbonyloxycholest-5-ene (518 mg, 1 m mole) in dry hexane (10 ml), 1,3-dibromo-5,5-dimethylhydantoin (172 mg, 0.6 m moles) was added dropwise under stirring and heating at oil bath temperature of 95° C., and the mixture was continued to react under the irradiation of infrared rays for 15 minutes. The reaction mixture was cooled, and the resulting precipitate was removed by filtration, the filtrate was concentrated at reduced pressure at 40° C. to afford a residual product. Xylene was added to this substance to form a solution. The resulting solution was added dropwise to a solution held at 170° C. of s-collidine (2.5 ml) in dry xylene (3 ml), and the reaction was carried out for additional 20 minutes. After the reaction, the resulting precipitate was removed by filtration and the filtrate was concentrated under reduced pressure at 40° C. to give residual product. The product was dissolved in ethylacetate (20 ml). The ethylacetate solution was washed with 1 N hydrochloric acid (3×10 ml), saturated sodium bicarbonate and water, and dried over anhydrous sodium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure to give 479 mg of residual product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388243
Source datasetuspto-grants-1983_06
ORD IDord-93df548d4a554e4fa2f6d8583f9c2b45
Source noteuspto-grants-1983_06