HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Phenylsuccinic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-cyano-3-phenylpropanoate | HCID 12414061 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenylsuccinic acid | HCID 95459 | 89% |
Reaction Steps
A mixture of 43.5 g (214 mmol) of ethyl 3-cyano-3-phenylpropanoate and 52.2 g (930.4 mmol) of potassium hydroxide in 670 mL of EtOH is refluxed for 4 hours. After cooling to room temperature, the medium is concentrated under vacuum and then treated with 1 L of 1N HCl, and a precipitate then forms, which is filtered off and rinsed with water (2×50 mL). The solid obtained is taken up in a mixture of 200 mL of toluene and 40 mL of EtOH and concentrated under reduced pressure, and then dried with a vane pump. 37 g of 2-phenylbutanedioic acid are obtained in the form of a solid, which is used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541455B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-9606fc799fc148db8f11487efd069dc2 |
| Source note | uspto-grants-2013_09 |