HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870952Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 54712370, compound
https://huagongshe.com/reaction/1870952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3-Nitrophenylacetic acid | HCID 15876 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 54712370 | HCID 54712370 | 58% |
Reaction Steps
3-Nitrophenylacetic acid (7.20 g, 39.6 mmol) and then dicyclohexylcarbodiimide (8.6 g, 42 mmol) were added to a 1,2-dichloroethane (100 ml) suspension of 4-hydroxy-6-methyl-2-pyrone (5.00 g, 39.6 mmol) at room temperature, then 4-dimethylaminopyridine (0.24 g, 2.0 mmol) added and stirring carried out for 1 hour at 60° C., after which further 4-dimethylaminopyridine (0.48 g, 4.0 mmol) was added and stirring performed for 6 hours at 60° C. While the solution was still warm, the dicyclohexylurea was filtered off, and the reaction solution washed with dilute hydrochloric acid (50 ml), after which the aqueous layer was extracted with dichloromethane. After drying with anhydrous sodium sulphate, the solvent was distilled off and separation and purification carried out column chromatography. When recrystallization was performed from ethanol, 4-hydroxy-6-methyl-3-(3-nitrophenylacetyl)-2-pyrone (6.60 g, 58%) was obtained as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06100292 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-4e421ddabbce49429d3c388c3f5bed61 |
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| Source note | uspto-grants-2000_08 |
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