HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292328Generated: October 31, 2026
Triethylamine → 3-[3,4-Bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide
https://huagongshe.com/reaction/2292328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Chlorocarbonyl)-1,2-phenylene diacetate | HCID 14096948 | — |
| Reactant | 3-Amino-2-oxo-1-imidazolidinecarboxamide, monohydrochloride | HCID 131715832 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[3,4-Bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide | HCID 14390896 | 314.9% |
Reaction Steps
3-Amino-2-oxo-1-imidazolidinecarboxamide, monohydrochloride (12 g 0.006 mol) was suspended in 300 ml of dichloromethane. The suspension was cooled to 0° C. and 29.2 ml of triethylamine (0.198 mol) was added; the mixture was stirred for another 20 minutes. [3,4-Bis(acetyloxy)benzoyl]chloride (10.5 g) dissolved in 200 ml of dichloromethane was added dropwise with stirring at 0° C. and the mixture was stirred overnight at room temperature, filtered and treated with 50 ml of water. After stirring for 5 minutes, 3-[3,4-bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide crystallized out (7.2 g) contaminated with some triethylamine hydrochloride. The impurity was removed by treatment with water to yield 6.6 g of 3-[3,4-bis(acetyloxy)benzoyl]-2-oxo-1-imidazolidinecarboxamide, melting point 222°-224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801705 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-1eb977fc06264829a978e9537a5daabf |
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| Source note | uspto-grants-1989_01 |
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