HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555346Generated: October 29, 2026
tert-Butanol → 1-Benzyl-4-(N-Boc-amino)piperidine
https://huagongshe.com/reaction/555346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-Benzyl-4-(N-Boc-amino)piperidine | HCID 4438618 | 82.8% |
Reaction Steps
1-Benzylpiperidin-4-ylamine (3 g, 15.8 mmol), the starting material, was dissolved in 1M aqueous sodium hydroxide solution (35.8 ml) and t-butanol (32 ml) in a 250 ml vessel, and t-butyl-dicarbonate ((t-Boc)2O; 3.79 g, 17.38 mmol) was added thereto while stirring, and the resulting mixture was reacted at room temperature for 12 hrs. After the completion of reaction, the reaction mixture was extracted with ethyl acetate twice. Then, the organic layer was washed with 0.1N hydrochloric acid solution and brine in order, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue thus obtained was purified with a silica gel column chromatography to obtain 3.80 g of the title compound as a white solid (82.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08053435B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-1bc73f53efec4300b220744484a65aea |
|---|
| Source note | uspto-grants-2011_11 |
|---|