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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417565Generated: October 26, 2026

1,3-Dibromo-5,5-dimethylhydantoin → 2-Bromo-1-isopropyl-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1417565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Isopropyl-4-(trifluoromethyl)benzeneHCID 599680—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-isopropyl-4-(trifluoromethyl)benzeneHCID 54018878—

Reaction Steps

Using the general conditions described by H. Eguchi, H. Kawaguchi, S. Yoshinaga, A. Nishida, T. Nishiguchi, and S. Fujisaki (Bull. Chem. Soc. Jpn.., 1994, 67, 1918-1921), 1,3-dibromo-5,5-dimethylhydantoin (454 mg, 3.18 mmol) was added in one portion to a solution of 4-isopropyl-1-(trifluoromethyl)benzene (500 mg, 2.65 mmol) and trifluoromethanesulfonic acid (0.281 mL, 3.18 mmol) in dichloromethane (5.0 mL). The mixture was stirred in the dark at RT for 3 h. Saturated aqueous sodium bisulfite was added to the reaction mixture until the brown organic layer was decolorized. The mixture was neutralized by the addition saturated aqueous sodium bicarbonate solution (100 mL). The organic layer was separated, dried over sodium sulfate, and evaporated. The crude material was filtered through a column packed with silica gel and eluted with hexane to isolate a mixture containing the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877191
Source datasetuspto-grants-1999_03
ORD IDord-77a56d47bdec4597b5a6ec7268cf9eb8
Source noteuspto-grants-1999_03