HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → Methyl 4,4-ethylenedioxy-3-methyl-butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl 3-methyl-4-oxobutanoate | HCID 11804788 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 4,4-ethylenedioxy-3-methyl-butanoate | HCID 20305753 | — |
Reaction Steps
A mixture of methyl 3-methyl-4-oxo-butanoate (86.3 g), ethylene glycol (61.75 g, 0.996 m), p-toluenesulfonic acid (1 g) and benzene (700 ml) is refluxed under nitrogen for 16 hours. The resulting mixture is allowed to cool to room temperature and treated with ether (300 ml). The organic phase is washed with 5% sodium bicarbonate solution (100 ml), dried (Na2SO4) and evaporated in vacuo to give methyl 4,4-ethylenedioxy-3-methylbutanoate as a crude product (63.2 g). This material is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237054 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-4391e1b870f9420880c8af9d328f3771 |
| Source note | uspto-grants-1980_12 |