HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 23093701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 23093706 | HCID 23093706 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 23093701 | HCID 23093701 | 99% |
Reaction Steps
To a solution of 209 mg of tert-butyl 4-{(E)-2-[4-(butoxycarbonyl)-2,6-dimethylphenyl]vinyl}piperidine-1-carboxylate in 5 ml of ethanol, 1.5 ml of 1N aqueous sodium hydroxide solution was added, followed by stirring at ambient temperature for 3.5 hours. After 1 ml of tetrahydrofuran was added to the reaction mixture, the mixture was stirred at 50° C. overnight. The solvent was evaporated under reduced pressure, water and 1.6 ml of 1N hydrochloric acid were added thereto. The formed precipitates were collected by filtration and dried to give 179 mg of 4-{(E)-2-[1-(tert-butoxycarbonyl)piperidin-4-yl]vinyl}-3,5-dimethylbenzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044206B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-31933cd66cdc4fe7b42e928310ac2f9c |
| Source note | uspto-grants-2011_10 |