HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Chlorophenyl)-2-(4-chlorophenyl)ethanone → 2-Bromo-1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Chlorophenyl)-2-(4-chlorophenyl)ethanone | HCID 348312 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone | HCID 17748138 | — |
Reaction Steps
29.54 g of phenyltrimethylammonium tribromide are added to a solution of 20.83 g of 1-(2-chlorophenyl)-2-(4-chlorophenyl)ethanone in THF. The homogeneous solution is stirred at room temperature for 1 hour 15 minutes. The reaction medium is filtered and concentrated to dryness. The crude reaction product is taken up in dichloromethane and washed successively with water, with aqueous Na2CO3 solution and then with water. The organic phase is dried over Na2SO4, filtered and concentrated to dryness by distilling off the solvent under reduced pressure. The product is obtained in the form of an oil that crystallizes slowly. The crystals are washed with a minimum amount of ethanol to give the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618991B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-c5d7157c024e456fb8a3d99fec778240 |
| Source note | uspto-grants-2009_11 |