HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-hydroxy-3-(4-methoxyphenyl)-2-methylpropanoate → Ethyl 3-(4-methoxyphenyl)-2-methylprop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-hydroxy-3-(4-methoxyphenyl)-2-methylpropanoate | HCID 312882 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 3-(4-methoxyphenyl)-2-methylprop-2-enoate | HCID 53711494 | — |
Reaction Steps
A mixture of 71.8 g (0.30 mole) of ethyl β-(p-methoxyphenyl)-β-hydroxy-α-methylpropionate is refluxed with 41.0 g (0.30 mole) of potassium hydrogen sulfate in 718 ml of benzene for 1 hour. The insoluble white crystals formed are filtered off, washed with benzene and the solvent of the filtrate is removed on evaporation. This is dissolved in 700 ml of ether. The ether solution is washed with 4 × 100 ml of cold water until neutral followed by 80 ml of saturated sodium chloride solution, then it is dried over magnesium sulfate for 1.5 hours and filtered. The solvent is removed on an evaporator to give ethyl p-methoxy-α-methylcinnamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061771 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-39daad5a7252463c95e3a8965db6eb2c |
| Source note | uspto-grants-1977_12 |