HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → Methyl (2-ethyl-1,3-dioxolan-2-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl 3-oxovalerate | HCID 121699 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl (2-ethyl-1,3-dioxolan-2-yl)acetate | HCID 13085711 | 42.5% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of methyl 3-oxopentanoate (3 g, 23.1 mmol) in toluene (30 mL) was added ethane-1,2-diol (3 mL, 70.2 mmol) and p-toluenesulfonic acid (500 mg, 2.91 mmol), the resulting mixture was stirred at 120° C. overnight. Then the mixture was concentrated and partitioned between ethyl acetate and aqueous saturated sodium bicarbonate solution. The phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic phase was washed with brine and dried over sodium sulfate; then it was filtered and concentrated to give methyl 2-(2-ethyl-1,3-dioxolan-2-yl)acetate (1.7 g, 42.5%) as yellow oil which was used without purification. Product tlc [petroleum ether/ethyl acetate (15:1) developed with iodine, Rf 0.6]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359359B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-e9c4242b5d034850ac3265d3d78b1575 |
| Source note | uspto-grants-2016_06 |