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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579701Generated: October 30, 2026

Sodium borohydride → HCID 20136111, compound

https://huagongshe.com/reaction/579701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20136115HCID 20136115—
SolventIsopropanolHCID 3776—
ProductHCID 20136111HCID 20136111—

Reaction Conditions

Temperature40 °C

Reaction Steps

16.0 g (0.05 mol) of 1-methyl-3-[3-methyl-4-(1,1,2,2-tetrafluoroethoxy)phenyl]imidazolidine-2,4-dione are dissolved in 100 ml of isopropanol, and 2.85 g (0.075 mol) of sodium borohydride are added at a rate such that the temperature increases to 40° C. After the addition is complete, the mixture is stirred for a further 30 minutes at 40° C., and poured into 300 ml of ice-water. The mixture is extracted twice with 100 ml of methylene chloride in each case, and the combined methylene chloride phases are washed with 100 ml of water and dried over sodium sulfate. After removing the solvent by distillation, 15.4 g (96% of theory) of 4-hydroxy-1-methyl-3-[3-methyl-4-(1,1,2,2-tetrafluoroethoxy)phenyl]imidazolidin-2-one are obtained in the form of a pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749403
Source datasetuspto-grants-1988_06
ORD IDord-20d0a26371ee40f196fd2cd70dcd438e
Source noteuspto-grants-1988_06