HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884549Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 23506182, compound
https://huagongshe.com/reaction/1884549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | 9-Carboxyfluorene | HCID 74809 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23506182 | HCID 23506182 | 69% |
Reaction Steps
A mixture of 1,3-dimethylbarbituric acid (2.5 g, 16.01 mmol), 9-fluorenylcarboxylic acid (5.05 g, 24.01 mmol), 4-dimethylaminopyridine (0.98 g, 8.00 mmol) in dry CH2Cl2 (15 ml) was cooled to 0° C. and 1,3-dicyclohexylcarbodiimide (3.30 g, 16.01 mmol) added. The reaction mixture was stirred at room temperature overnight and filtered. The solid was washed with CH2Cl2 (50 ml) and the combined solution was washed with 2 N HCl solution (5 ml). The organic phase was dried over MgSO4 and evaporated. The residue was crystallised from recrystallised from MeOH giving 5-(9-fluorenyl-carbonyl)-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione 5 (2.85 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06765089B1 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-07af5f3ab6cb4843810002b39aab699d |
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| Source note | uspto-grants-2004_07 |
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