HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 54710609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 21260725 | HCID 21260725 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54710609 | HCID 54710609 | — |
Reaction Steps
The 2.49 g (14.8 mmol) of 5-acetyl-2-furanacetic acid, 1.87 g (14.8 mmol) of 4-hydroxy-6-methyl-2-pyrone and 3.37 g (16.3 mmol) of DCC were suspended in 25 ml of chloroform, then 183 mg (1.50 mmol) of DMAP added and stirring carried out overnight at 60° C. The reaction liquid was cooled to room temperature and the insoluble material filtered off. The mother liquor was concentrated and the residue purified by column chromatography. The solid obtained was recrystallized from ethanol and Compound 13 (496 mg, 1.79 mmol, 12%) obtained. This was converted to the sodium salt with an equivalent quantity of sodium hydrogen carbonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184245B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-7847e04511854d6dacb3322be982dd82 |
| Source note | uspto-grants-2001_02 |