HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 4-(2-Bromo-1,1,2-trifluoroethoxy)-2-chlorophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 4-(2-Bromo-1,1,2-trifluoroethoxy)phenol | HCID 13228498 | — |
| Catalyst | Diphenyl sulfide | HCID 8766 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(2-Bromo-1,1,2-trifluoroethoxy)-2-chlorophenol | HCID 13228501 | — |
Reaction Steps
12.2 g of 4-(2-bromo-1,1,2-trifluoroethoxy)-phenol and 5 drops of diphenyl sulfide were dissolved in 30 ml of glacial acetic acid, and 6.1 g of sulfuryl chloride were added, a little at a time, at 25° C. After 3 hours at 25° C., the volatile components were removed, the residue was taken up with 300 ml of methylene chloride, and the solution was washed with 100 ml of 10% strength NaHCO3 solution and 100 ml of water, dried over Na2SO4 and distilled at 82° C./0.3 mbar. Yield: 12.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04551448 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-d2a3074b604c4089a52010e1c3aefd2c |
| Source note | uspto-grants-1985_11 |