HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450793Generated: October 30, 2026
Dimethylformamide → HCID 59478382, compound
https://huagongshe.com/reaction/450793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-Furancarboxylic acid, 5-methyl- | HCID 74710 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59478382 | HCID 59478382 | 38.6% |
Reaction Steps
A mixture of 5.05 g of 5-methyl-2-furanecarboxylic acid, 7.14 g of CDI, and 40 mL of DMF was stirred at 50° C. for 2 hours. To the reaction solution were added 6.71 g of DBU and 6.53 g of 2-methyl-2-propanol at room temperature, followed by stirring at 50° C. for 48 hours. The reaction solution was concentrated under reduced pressure, and the obtained residue was diluted with diethyl ether and washed with a 5% aqueous ammonium chloride solution, a saturated aqueous sodium hydrogen carbonate solution, and then a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain 2.82 g of tert-butyl 5-methyl-2-furanecarboxylate as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08486970B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-713fca1309b84fc4a2085c228f15ab1f |
|---|
| Source note | uspto-grants-2013_07 |
|---|