HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1,3-Butanedione, 1-(2-furanyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 2-furoate | HCID 11902 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,3-Butanedione, 1-(2-furanyl)- | HCID 12168 | 99.6% |
Reaction Steps
4.27 ml (5.04 g, 40 mmol) methyl 2-furoate was added to a suspension of NaH (made from 3.83 g commercial NaH slurry by removal of the mineral oil with pentane) in 30 ml anhydrous diethyl ether. To this was added, so as to maintain the temperature below 30° C., 5.87 ml (4.64 g, 80 mmol) acetone (dried over CaCl2). This mixture was heated under reflux for 2 h, cooled, and divided between diethyl ether and 3M HCl. The ether layer was washed with brine, dried (MgSO4), and concentrated to yield 6.06 g of a red oil (raw yield 99%) which was purified by vacuum distillation (b.p. 85°-90° C./1 torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631374 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-8c764efa47ef4b9b8b9f366061dd03f4 |
| Source note | uspto-grants-1997_05 |