HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579701Generated: October 30, 2026
Sodium borohydride → HCID 20136111, compound
https://huagongshe.com/reaction/579701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20136115 | HCID 20136115 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 20136111 | HCID 20136111 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749403 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-20d0a26371ee40f196fd2cd70dcd438e |
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| Source note | uspto-grants-1988_06 |
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