HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656009Generated: October 31, 2026
4-(Trifluoromethoxy)aniline → p-(Trifluoromethoxy)phenol
https://huagongshe.com/reaction/1656009
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethoxy)aniline | HCID 600848 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | p-(Trifluoromethoxy)phenol | HCID 70015 | 70.2% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05252597 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-8a94da0498b446a2820ea3646e878664 |
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| Source note | uspto-grants-1993_10 |
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