HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4,5-Dimethyl-2-furaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2,3-Dimethylfuran | HCID 34337 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5-Dimethyl-2-furaldehyde | HCID 643406 | 76% |
Reaction Steps
According to the procedure of S. F. Martin, et al. J. Org. Chem. 1984, 49, 2512-2516, phosphorus oxychloride (10.7 mL, 114.4 mmol) was added dropwise to a stirred, ambient temperature solution of 2,3-dimethylfuran (10 g, 104 mmol) in DMF (150 mL) under a dry nitrogen atmosphere over a period of 30 min. After 3 h., the reaction mixture was hydrolized with 2.5 N aq. sodium hydroxide and further diluted with water (50 mL). Aqueous mixture was extracted with dichloromethane (2×300 mL). The combined dichloromethane extracts were washed with water, dried with brine and purified by silica gel flash chromatography (eluent: ethyl acetate) to provide a yellow oil (9.8 g, 76%); MS (ESI): [M+H]+, 125.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057316 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-f6996d1a08d04e1da4f54ba7347c4ec2 |
| Source note | uspto-grants-2000_05 |