HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 33185-56-7
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 10176652 | HCID 10176652 | — |
| Solvent | Water | HCID 962 | — |
| Product | 33185-56-7 | HCID 10176507 | 46% |
Reaction Steps
A mixture of 4.69 g of 2-methoxyphenyl trifluoromethyl sulfide, obtained according to Example 3, 20 ml of 48% strength by weight aqueous hydrobromic acid, and 20 ml of 96% strength by weight acetic acid was boiled under reflux for 24 hours. The completion of the reaction was then checked by gas chromatography. After cooling, the reaction mixture was poured into water. The organic phase was separated off and the aqueous phase was extracted with dichloromethane. The extract was combined with the organic phase. Drying over magnesium sulfate, concentration, and vacuum distillation gave 2.01 g (46% of theory) of 2-hydroxyphenyl trifluoromethyl sulfide (boiling point 65-66° C. at 26 mbar, melting point 35-37° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06175042B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2bc00ae97c54417b98120ae06393c8f8 |
| Source note | uspto-grants-2001_01 |