HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Bromophenyl)(4-chlorophenyl)methanone → 4-Chloro-4'-isopropylbenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Bromophenyl)(4-chlorophenyl)methanone | HCID 2756868 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Catalyst | HCID 131730689 | HCID 131730689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-4'-isopropylbenzophenone | HCID 2757623 | 198% |
Reaction Steps
(4-bromophenyl)(4-chlorophenyl)methanone (10.0 g, 12.3 mmol) and bis(diphenylphosphino)propane nickel(II) chloride (0.4 g, 0.7 mmol) were dissolved in purified tetrahydrofuran (200 mL) under a nitrogen atmosphere, and isopropyl magnesium chloride (18.7 mL, 37.4 mmol) was slowly added thereto at 0° C. The reaction mixture solution was stirred at room temperature for 24 hours. The reaction mixture solution was subjected to extraction with dichloromethane and distilled water, and the extracted material was subjected to column chromatography (hexane:ethylacetate=8:2). The reaction solvent was removed, and then the residue material was dried in vacuum to thereby obtain a white solid (6.3 g, yield: 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476474B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-a921723b4f7c4fc99175605abb39d337 |
| Source note | uspto-grants-2013_07 |