HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 54702828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 21260728 | HCID 21260728 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54702828 | HCID 54702828 | — |
Reaction Steps
1.50 g (9.73 mmol) of the 4,5-dimethyl-2-furanacetic acid, 1.22 g (9.67 mmol) of 4-hydroxy-6-methyl-2-pyrone and 2.22 g (10.7 mmol) of DCC were suspended in 30 ml of chloroform, then 244 mg (2.0 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 then concentrated and the residue purified by column chromatography. The solid obtained was recrystallized from diethyl ether, and Compound 7 (488 mg, 186 mmol, 19%) 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-475d8b680fa145ac813246da4240cf28 |
| Source note | uspto-grants-2001_02 |