HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-Fluorophenoxy)-1-(3-phenylpyrrolidin-1-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4-Fluorophenoxy)acetyl chloride | HCID 2759057 | — |
| Reactant | 3-Phenylpyrrolidine | HCID 3146743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Fluorophenoxy)-1-(3-phenylpyrrolidin-1-yl)ethanone | HCID 2927893 | 82.7% |
Reaction Steps
A solution of 3-phenylpyrrolidine (294 mg, 2 mmol) in dry dichloromethane (6 mL) is cooled in an ice bath, and (4-fluoro-phenoxy)-acetyl chloride (471.5 mg, 2.5 mmol, 1.25 eq) and triethylamine (417 μL, 3 mmol, 1.5 eq) are added. After stirring for 6 hours at room temperature the reaction mixture is diluted with dichloromethane (10 mL). The organic solution is subsequently washed with 1 M KHSO4, 5% NaHCO3 and brine. After drying over Na2SO4, dichloromethane is removed in vacuo and the crude material is purified by flash chromatography (silicagel, ethyl acetate/toluene 1:4). The fractions containing 2-(4-fluorophenoxy)-1-(3-phenylpyrrolidin-1-yl)ethan-1-one are collected and the solvent is removed in vacuo to give 495 mg of colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912329B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-489236a76b854f4b82142f7c9377b575 |
| Source note | uspto-grants-2014_12 |