HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 22248434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl 4-[(2-aminophenoxy)methyl]piperidine-1-carboxylate | HCID 22248383 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22248434 | HCID 22248434 | 100% |
Reaction Steps
After dissolving 400 mg of 1-(tert-butoxycarbonyl)-4-(2-aminophenoxymethyl)piperidine in 10 ml of tetrahydrofuran, 0.15 ml of acetic anhydride and 0.24 ml of triethylamine were added and the mixture was stirred overnight at room temperature. The reaction solution was filtered with silica gel and NH silica gel. The solvent was distilled off under reduced pressure to obtain the title compound (459 mg, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915274B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-fe2dd575ea5747998aea5892d2344a8a |
| Source note | uspto-grants-2011_03 |