HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284119Generated: October 25, 2026
Phosgene → 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone
https://huagongshe.com/reaction/1284119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Acetylimidazolidinone | HCID 79350 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone | HCID 11229265 | — |
Reaction Steps
20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978056 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-7cc0f47e459d41969c9cc6c710a80aa9 |
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| Source note | uspto-grants-1976_08 |
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