HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-[4-(2-Tert-butyl-4-methylphenyl)piperazin-1-yl]-3-oxopropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl 3-[4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl]-3-oxopropanoate | HCID 66750839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[4-(2-Tert-butyl-4-methylphenyl)piperazin-1-yl]-3-oxopropanoic acid | HCID 66751329 | 96% |
Reaction Steps
To a stirred solution of ethyl 3-[4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl]-3-oxopropanoate (Example 83, 0.210 g, 0.61 mmol) in THF (5 mL) stirring at 0° C. was added 1 M lithium hydroxide solution (5 mL, 5 mmol). After 2 h the reaction mixture was acidified with 1 M hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and the solvent was to evaporated under reduced pressure to provide 3-[4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl]-3-oxopropanoic acid (0.186 g, 96%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-46aa5fa2ce6043a08fd820e879a900be |
| Source note | uspto-grants-2014_10 |