HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenol → HCID 18669510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10551830 | HCID 10551830 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18669510 | HCID 18669510 | 100.5% |
Reaction Steps
To a solution of N,N-dibenzyl-4-(2-bromoacetyl)benzenesulfonamide (10.5 g, 23 mmoles), and p-chlorophenol (2.94 g, 23 mmoles) in methylene chloride (42 ml), potassium carbonate (4.83 g, 34.7 mmoles) and tetrabutylammonium bromide (0.42 g, 1.2 mmoles) in water (140 ml)was added. The reaction mixture was refluxed for 16 hours. After cooling, the mixture was diluted with methylene chloride (150 ml). The organic layer was separated, washed with water, and dried (Na2SO4) The solvent was removed under reduced pressure. N,N-dibenzyl-4-[2-(4-chlorophenoxy)acetyl]benzenesulfonamide (11.7 g) was obtained as a semisolid residue, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518303B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-35e2601fbfe44f2fbe17e0a2fad0a240 |
| Source note | uspto-grants-2003_02 |