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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166679Generated: November 3, 2026

1,3-Dibromo-5,5-dimethylhydantoin → HCID 53734901, compound

https://huagongshe.com/reaction/2166679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantHCID 54438691HCID 54438691—
SolventO-XyleneHCID 7237—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 53734901HCID 5373490186.1%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 1α,3β-diethoxycarbonyloxy-25-hydroxycholesta-5-ene (562 mg, 1 m mole) in dry hexane (10 m), 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 482 mg of residual product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388243
Source datasetuspto-grants-1983_06
ORD IDord-1ab5a281775d42ceb1878b6fa5609f63
Source noteuspto-grants-1983_06