HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436622Generated: October 28, 2026
2-Imidazolidinone → HCID 21453127, compound
https://huagongshe.com/reaction/436622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Imidazolidinone | HCID 8453 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21453127 | HCID 21453127 | — |
Reaction Steps
A suspension, cooled to 0° C, of imidazolidin-2-one (17.2 parts by weight) in tetrahydrofurane (200 parts by volume) was treated dropwise over the course of one hour, with pivaloyl chloride (24.2 parts by weight) at the same temperature. The mixture was then stirred for a further 3 hours at 0° C, triethylamine (27.8 parts by volume) was subsequently added dropwise while cooling with ice water, and the mixture was then left to stand overnight at room temperature. The triethylamine hydrochloride which had separated out was then filtered off, the filtrate was completely concentrated in vacuo by means of a rotary evaporator and the residue was further warmed for 1 hour, in vacuo, in a bath at 60° C. The oily product (crude yeild: 32.8 parts by weight) was further processed, as it was. When an attempt was made to distill the substance in vacuo, severe decomposition occurred.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009272 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-9768e4fdc1e04982be2388db72d9597c |
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| Source note | uspto-grants-1977_02 |
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