Hydrochloric Acid → HCID 86065127, compound
Reaction equation
[Na+].[F:2][C:3]([F:16])([F:15])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][S:11]([O-:14])(=[O:13])=[O:12].Cl>CO>[F:16][C:3]([F:2])([F:15])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][S:11]([OH:14])(=[O:13])=[O:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -20 °C
Procedure
(2-Trifluoromethylphenyl)methanesulfonic acid sodium salt (22.2 g, 84 mmol) was suspended in MeOH (950 mL) and cooled to −20° C. At that temp with continued cooling HCl (g) was bubbled through the mixture for 5 min. The resulting white suspension was stirred at room temperature for 1.5 h, then cooled in an ice-bath. The resulting suspension was filtered and the collected solid allowed to air-dry overnight to afford (2-trifluoromethylphenyl)methanesulfonic acid (20.3 g, ˜100%), a white solid, which was used without further purification
Workup
- customwas bubbled through the mixture for 5 min
- temperaturecooled in an ice-bath
- filtrationThe resulting suspension was filtered
- customto air-dry overnight
Sources & evidence
- ORD record
- ord-05b8f58bd65249279a4481aa15abdc0f
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557135B2
Reaction notes
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