HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(3-Fluoro-4-methoxyphenyl)propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Fluoro-4-methoxybenzonitrile | HCID 2774548 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | 1-(3-Fluoro-4-methoxyphenyl)propan-1-one | HCID 276284 | 57% |
Reaction Steps
To a solution of 3-fluoro-4-methoxybenzonitrile (350 mg, 2.32 mmol) in 15 mL anhydrous THF was added ethylmagnesium bromide (1 M in Et2O, 4.63 mL) at 0° C. The reaction mixture was stirred at rt overnight, then quenched with sat. NaHCO3, extracted with EtOAc, washed with brine, dried and evaporated. The residue was purified by column chromatography (eluent: petroleum ether/EtOAc=5/1) over silica gel to give the product (239 mg, 57% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309211B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-0a004a23c6b942cc9d969021f2c78999 |
| Source note | uspto-grants-2016_04 |