HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 1-[2-(2-Fluorophenoxy)ethyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-[2-(2-Fluorophenoxy)ethyl]piperazine-1-carboxylic acid tert-butyl ester | HCID 67298803 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(2-Fluorophenoxy)ethyl]piperazine | HCID 762703 | 84% |
Reaction Steps
The above oil of 4-[2-(2-fluorophenoxy)ethyl]piperazine-1-carboxylic acid tert-butyl ester (4.0 g, 12 mmol) in dichloromethane (60 mL) was mixed with trifluoroacetic acid (10 mL) and was stirred at room temperature for 2 hours. The solvent was evaporated and the residue was treated with a saturated solution of NaHCO3. The aqueous solution was extracted with dichloromethane and the organic layer was concentrated to give 1-[2-(2-fluoro-phenoxy)ethyl]piperazine as a white solid (2.25 g, 84%). 1H NMR (400 MHz, DMSO-d6): δ 2.40 (b, 4H), 2.67 (m, 6H), 4.13 (t, 2H), 6.92 (m, 1H), 7.11 (t, 1H), 7.18 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183374B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-ef5a76abbb6543008a7d7529704b5885 |
| Source note | uspto-grants-2012_05 |