HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 4-Chloro-3-(trifluoromethoxy)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 3-(Trifluoromethoxy)phenol | HCID 2733261 | — |
| Product | 4-Chloro-3-(trifluoromethoxy)phenol | HCID 17750695 | — |
Reaction Steps
A solution of 3-trifluoromethoxyphenol and sulfuryl chloride is stirred at room temperature until conversion of starting material to product is complete. The excess of sulfuryl chloride is evaporated using a rotary evaporator. The residue is dissolved in dichloromethane and washed with water. The organic layer is separated, dried over MgSO4, filtered and concentrated to yield crude 4-chloro-3-trifluoromethoxyphenol. The crude product is purified over a silica gel column using to give purified product that is used with or without further purification in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563792B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-8df28892e37a4ce3ad6acd462b0ed174 |
| Source note | uspto-grants-2009_07 |