HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorobenzyl chloride → 4-(3,4-Dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Fluoro-4-biphenylyl acetone | HCID 12950418 | — |
| Product | 4-(3,4-Dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanone | HCID 19073613 | 85% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
45.1 g of the ketone compound thus obtained, 50.3 g of 3,4-dichlorobenzyl chloride and 15.8 g of sodium hydroxide were mixed, heated with stirring at 100° C. for 6 hours. The reaction solution was left to cool to room temperature and then extracted by an addition of ethyl acetate and water. The organic layer was post-treated by a conventional method. Then, the product was purified by silica gel column chromatography (hexane/ethyl acetate=50/1) to obtain 65.0 g (yield: 85%) of 4-(3,4-dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616803 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-1add2f6c5621410ab3b61f86e55ce5fc |
| Source note | uspto-grants-1997_04 |