HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474583Generated: October 30, 2026
3-(Trifluoromethyl)phenol → 4-(3-(Trifluoromethyl)phenoxy)benzaldehyde
https://huagongshe.com/reaction/474583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-(Trifluoromethyl)phenoxy)benzaldehyde | HCID 12148788 | 85.4% |
Reaction Steps
K2CO3 (23.45 g, 170 mmol) was added to a solution of 3-(trifluoromethyl)phenol (25 g, 154 mmol) and 4-fluorobenzaldehyde (19.14 g, 154 mmol) in DMF (300 mL), and the reaction mixture was stirred at 140° C. for 4 h. After cooling down to room temperature, the reaction mixture was poured into ice water (2500 ml), extracted with ethyl acetate (500 ml×2), and washed with brine (200 mL×2). The organic phase was dried with sodium sulfate, filtered, and concentrated to give the title compound as a brown solid (35 g, 66.9% yield). LCMS: rt=1.62 min, [M+H+]=267
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637536B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-9cbcd44b53eb424398e9a97c27f0bb8a |
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| Source note | uspto-grants-2014_01 |
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