HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Bromophenyl)acetaldehyde → 1-(2-Bromophenyl)butan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Bromophenyl)acetaldehyde | HCID 11424180 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Bromophenyl)butan-2-ol | HCID 60799136 | — |
Reaction Steps
To a solution of 2-(2-bromophenyl) acetaldehyde (15 g, 75.37 mmol) in THF (100 ml) was added propyl magnesium bromide (1.0 M in THF) (15.13 g, 113.6 mmol) at 0° C. then stirred at RT for 3 h. The reaction mixture was quenched with ammonium chloride then the title compound was purified by separation methods A, E and M. (Yield 7.0 g). The enantiomer showed up at tr=13.6 min with Chiralcel OJH (4.6×250 mm) 5μ, hexane:ethanol (98:02), 1 ml/min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249127B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-a05ba5b8246a46649122c434265a6137 |
| Source note | uspto-grants-2016_02 |