HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133832Generated: October 27, 2026
Acetic Acid → Diethyl (3-methyl-2,5-dioxoimidazolidin-4-yl)phosphonate
https://huagongshe.com/reaction/133832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 1-Methylhydantoin | HCID 69217 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl (3-methyl-2,5-dioxoimidazolidin-4-yl)phosphonate | HCID 13937024 | — |
Reaction Steps
A mixture of 1-methylhydantoin (20.25 g, 180 mmole) and acetic acid (100 ml) is heated to 90° C. Bromine (10 ml, 195 mmole) is introduced dropwise at such a rate that instant decolorization occurred. After the addition is completed, the reaction mixture is stirred at 90° C. for 60 minute and at room temperature overnight. The acetic acid is decanted from white precipitate and removed in vacuo. The residue is combined with the precipitate and suspended in diethylether (200 ml). Triethylphosphite (32 ml, 180 mmole) is added portionwise with stirring and cooling. A solution resulted which on continued stirring, yield trace of white precipitate. The mixture is diluted with diethyl ether and allowed to stand overnight. Decanted the solvent, and pumped in vacuum oven to give white crystal ylide, (3-Methyl-2,5-dioxo-imidazolidin-4-yl)-phosphonic acid diethyl ester: 16.57 g (36.8%) MS(ES+): (M+H)=251.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07390910B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-32856a950cec45fb8dbe459aae6a97c8 |
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| Source note | uspto-grants-2008_06 |
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