HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzaldehyde → 1-(2-Bromophenyl)prop-2-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Bromophenyl)prop-2-en-1-ol | HCID 19102220 | 91.3% |
Reaction Steps
To a solution of allylmagnesium bromide (108 mL, 108 mmol, 2.0 eq) in THF was added a solution of 2-bromobenzaldehyde (10 g, 54 mmol, 1.0 eq) in THF (20 mL) dropwise at −18° C. The mixture was allowed to reach room temperature for 17 h, then, quenched with saturated NH4Cl aqueous. The mixture was partitioned between brine and ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to provide 1-(2-bromophenyl)prop-2-en-1-ol (10.5 g, 91%). LC-MS (m/z)=213.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422271B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-21114ca439ff42f0ae7bd97e98d99433 |
| Source note | uspto-grants-2016_08 |