4-(Trifluoromethoxy)aniline → p-(Trifluoromethoxy)phenol
Reaction equation
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:10]=[CH:9][C:7](N)=[CH:6][CH:5]=1.N([O-])=[O:14].[Na+]>OS(O)(=O)=O>[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:10]=[CH:9][C:7]([OH:14])=[CH:6][CH:5]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
p-Trifluoromethoxy aniline (49.60 g) was added rapidly dropwise to vigorously stirred 9N aqueous H2SO4 (500 mL) at 40° C. The mixture was heated to dissolve the solid, then cooled to 0° C. To the fine white suspension, a solution of sodium nitrite (19.46 g in 50 mL of H2O) was added portionwise until an immediate positive KI/starch test result was obtained. This cold solution of diazonium salt was added rapidly dropwise to 9N aqueous H2SO4 (500 mL) at 110° C. Stirring and heating was continued for 2.5 hours. The mixture was cooled to 10° C. and extracted with diethyl ether (3×500 mL). The combined organic layers were dried (MgSO4), filtered and evaporated in vacuo, then flash chromatographed on SiO2 using diethyl ether as eluant to give 35.0 g of the desired phenol as a light brown oil. The oil was distilled (b.p.=75°-80° C. at 20 torr.) to afford a yellow liquid.
Workup
- temperatureThe mixture was heated
- dissolutionto dissolve the solid
- customresult
- customwas obtained
- temperatureheating
- temperatureThe mixture was cooled to 10° C.
- extractionextracted with diethyl ether (3×500 mL)
- dry with materialThe combined organic layers were dried (MgSO4)
- filtrationfiltered
- customevaporated in vacuo
- customflash chromatographed on SiO2
Sources & evidence
- ORD record
- ord-5426fb49e68e4ba6b8c196b723ef12e9
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05047552
Reaction notes
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