HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Chloro-4-(trifluoromethoxy)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diphenyl sulfide | HCID 8766 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | p-(Trifluoromethoxy)phenol | HCID 70015 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-(trifluoromethoxy)phenol | HCID 13044783 | 92% |
Reaction Steps
0.05 part by weight of diphenyl sulfide is added to a solution of 8.9 parts by weight of 4-trifluoromethoxyphenol in 30 parts by weight of glacial acetic acid, and 6.8 parts by weight of sulfuryl chloride are then added dropwise, without cooling. The mixture is subsequently stirred at room temperature for 3 hours, the solvent is stripped off and the residue is taken up in 50 parts by weight of methylene chloride. This solution is twice washed with 50 parts by weight of saturated bicarbonate solution, and is dried and concentrated. Distillation of the residue under reduced pressure gives 9.8 parts by weight (92% of theory) of 2-chloro-4-trifluoromethoxyphenol of boiling point 70° C./13 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04428944 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-0fc542c5f4064e8c9c068c1153210e55 |
| Source note | uspto-grants-1984_01 |