HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255852Generated: October 30, 2026
Carbon Dioxide → n-Propyl Cinnoline-4-carboxylate
https://huagongshe.com/reaction/255852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Cinnoline-4-carboxylic acid | HCID 89099 | — |
| Reactant | Imidazole sodium | HCID 57373095 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | n-Propyl Cinnoline-4-carboxylate | HCID 20164604 | — |
Reaction Steps
A suspension of 870 mg of 1, and 850 mg of carbonyidimidazole (CDII) in 30 ml of tetrahydrofuran (THF) was stirred at room temperature until CO2 evolution ceased (ca. 30 minutes). After being stirred for 2 hours, the resulting mixture was treated with 320 mg of dry nypropanol and 3 drops of a 0.1 M solution of sodium imidazole in THE. The mixture was held at room temperature overnight, then the solvent was evaporated and the residue was partitioned between water and ether. The etheral extract was washed with saturated sodium bicarbonate solution, then with brine, then dried (MgSO4) and stripped in a rotary evaporator. The residue was chromatographed over silica gel, using a 1:1 v:v mixture of cyclohexane and ethyl acetate as eluent, to give 5, as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04699651 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-e63f5621c93e4a72858163153f30ce58 |
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| Source note | uspto-grants-1987_10 |
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