HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 1-[2-(4-hydroxyphenoxy)ethyl]piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | 4-(2-Bromoethoxy)phenol | HCID 12833932 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 1-[2-(4-hydroxyphenoxy)ethyl]piperidine-4-carboxylate | HCID 57448391 | — |
Reaction Steps
To a stirred suspension of 4-(2-bromo-ethoxy)-phenol (600 mg, 2.77 mmol) and ethyl isonipecotate (470 μL, 3.06 mmol) in CH3CN (12 mL) was added Et3N (768 μL, 5.54 mmol). The resultant mixture was stirred at rt overnight and then concentrated to afford the title compound, which was used immediately in the next step. MS (ESI): mass calcd. for C16H23NO4, 293.16; m/z found, 294.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939527B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-6b5970e75c0b4eb69c83f7c71f321063 |
| Source note | uspto-grants-2011_05 |