HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373732Generated: October 31, 2026
Nitric Acid → 4-Nitro-3,5-bis(trifluoromethyl)phenol
https://huagongshe.com/reaction/1373732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 3,5-Bis(trifluoromethyl)phenol | HCID 67680 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Nitro-3,5-bis(trifluoromethyl)phenol | HCID 21075599 | — |
| Product | 4-Nitro-3,5-bis(trifluoromethyl)phenol | HCID 21075602 | 59.3% |
Reaction Steps
Fuming nitric acid (8.22 mL, 198.2 mmol) was added dropwise to a solution of 3,5-bis(trifluoromethyl)phenol (28.5 g, 123.9 mmol) in acetic acid (300 mL) at about 10° C. After being elevated to room temperature, the mixture was stirred for 43 hours. The reaction mixture was poured into ice water and the resulting solution was extracted with ethyl acetate. The organic layers were combined, washed successively with water and saturated saline, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (developing solvent; hexane:acetone=15:1→10:1) to yield a crude product. The crude product thus obtained was subjected to sublimation separation under reduced pressure (3 mmHg) at 80° C. by using an evaporator to distill off the isomer, that is, 2-nitro-3,5-bis(trifluoromethyl)phenol, whereby 10.1 g (yield: 29.7%) of 4-nitro-3,5-bis(trifluoromethyl)phenol was obtained as yellow needle-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163944B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-ab342dc5df01417488f4ca28541588f7 |
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| Source note | uspto-grants-2007_01 |
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