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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392912Generated: October 29, 2026

Formaldehyde → 2-(Hydroxymethyl)-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/392912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHydrogen PeroxideHCID 784—
ReactantPropionic AcidHCID 1032—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-(Trifluoromethyl)phenolHCID 67874—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(Hydroxymethyl)-4-(trifluoromethyl)phenolHCID 2336312970.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803457B1
Source datasetuspto-grants-2004_10
ORD IDord-81500cb4265c40f2b2387409994cb0c0
Source noteuspto-grants-2004_10