HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → t-Butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate | HCID 21940085 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | t-Butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate | HCID 23371871 | 55.2% |
Reaction Steps
8.84 g (32.0 mmol) of t-butyl 4-(4-aminophenyl)-piperidine-1-carboxylate were dissolved in 150ml of methylene chloride and treated with 3.82 g (35.2 mmol) of ethyl chloroformate in the presence of 2.78 g (35.2 mmol) of pyridine. The reaction mixture was stirred at room temperature for 16 hours. Thereafter, it was washed with water and the organic phase was dried over sodium sulfate, filtered and evaporated. The residue (11.3 g) was chromatographed on 95 g of silica gel 60 with ether/n-hexane (4:6). After recrystallization from ether/n-hexane there were obtained 6.15 g of t-butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate. M.p.: 126°-128°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574055 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-f9830ce84748488ea495eb73b0c0a207 |
| Source note | uspto-grants-1996_11 |