HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → tert-butyl [(1S)-1-methyl-2-(piperidin-4-yloxy)ethyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | tert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate | HCID 57517478 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | tert-butyl [(1S)-1-methyl-2-(piperidin-4-yloxy)ethyl]carbamate | HCID 57517479 | 76.3% |
Reaction Steps
To a solution of tert-butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate (1.03 g) in acetic acid (10 mL)/ethanol (10 mL) was added platinum oxide (500 mg), and the reaction mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere. The catalyst was filtered off, and the filtrate was concentrated. The obtained residue was dissolved in 0.5 M hydrochloric acid, and the solution was washed with ethyl acetate, basified with potassium carbonate, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give the title compound (805 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703758B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-c348968e42ff4034a9b3259e6b2fa7c6 |
| Source note | uspto-grants-2014_04 |