HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromoacetophenone → HCID 25023178, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25023178 | HCID 25023178 | — |
Reaction Steps
To a solution of 1-(4-bromophenyl)ethanone (2.0 g, 10 mmol) and (S)-2-methylpropane-2-sulfinamide (1.2 g, 10 mmol) in THF (20 mL) was added Ti(OiPr)4 (5 mL). The reaction mixture was refluxed overnight. The mixture was quenched with sat. NH4Cl solution and diluted with EtOAc. The mixture was filtered through a pad of Celite and washed with EtOAc. The layers were separated and the organic layer was washed with brine, dried and concentrated to give the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309227B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-5b135a80b1f840bd81e056ce9e18669c |
| Source note | uspto-grants-2016_04 |