HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392912Generated: October 29, 2026
Formaldehyde → 2-(Hydroxymethyl)-4-(trifluoromethyl)phenol
https://huagongshe.com/reaction/392912
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Hydroxymethyl)-4-(trifluoromethyl)phenol | HCID 23363129 | 70.6% |
Reaction Steps
Paraformaldehyde (3.4 g, 0.114 mol) was added in 0.5 g portions over a six hour period to a refluxing mixture of 4-trifluoromethyl phenol (2.3 g, 0.0142 mol), phenyl boronic acid (2.1 g, 0.017 mol) and proprionic acid (530 μL, 7 mmol) in benzene with the azeotropic removal of water (Dean-Stark trap). When the addition was complete, the reaction was heated for an additional hour, then cooled with an ice bath, diluted with THF (30 mL) and treated with 5 mL of 30% hydrogen peroxide solution. After stirring for one hour, the mixture was partitioned between water (50 mL) and ethyl acetate (50 mL). The organic layer was washed with NaHSO3 solution (1×50 mL), brine (1×50 mL), dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (30% ethyl acetate/hexanes) to afford 950 mg (35%) of the title compound as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.42 (d, 1H, J=9.1 Hz); 7.3 (s, 1H); 6.95 (d, 1H, J=9.1 Hz); 4.89 (s, 2H);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06803457B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-81500cb4265c40f2b2387409994cb0c0 |
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| Source note | uspto-grants-2004_10 |
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