HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(3-Methoxypheny)-1-phenylpropanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-Bromo-2-(3-methoxyphenyl)ethane | HCID 137450 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178490129 | HCID 178490129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-Methoxypheny)-1-phenylpropanol | HCID 14224733 | — |
Reaction Steps
To a solution of benzaldehyde (920 μl, 9 mmol) in dry THF (20 mL) was added slowly a solution of 2-(3-methoxyphenyl) ethylmagnesium bromide prepared from 2-(3-methoxyphenyl) ethyl bromide (2.1 g. 9.77 mmol) and magnesium (300 mg, 12 mmol). The mixture was stirred at room temperature for ½ hour then quenched with saturated NH4Cl. The mixture was then extracted into EtOAc, washed with H2O, dried (Na2SO4), filtered and concentrated in vacuo, then purified by silica gel chromatography (30% EtOAc/Hexane) to provide the desired product as a colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-3ee10c20dc3a44fabeb57aae702fd5f5 |
| Source note | uspto-grants-2002_03 |