HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 54712964, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 222553-93-7 | HCID 21260742 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54712964 | HCID 54712964 | — |
Reaction Steps
The 3.82 g (22.4 mmol) of 3,5-dimethylthiopheneacetic acid, 2.87 g (22.7 mmol) of 4-hydroxy-6-methyl-2-pyrone and 5.13 g (24.8 mmol) of DCC were suspended in 70 ml of toluene, then 273 mg (2.23 mmol) of DMAP added and stirring carried out overnight at 90° 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 12 (684 mg, 2.45 mmol, 11%) 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-9c18844806ae4235805f5cacc03e9524 |
| Source note | uspto-grants-2001_02 |