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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071214Generated: November 4, 2026

Dimethylamine → 2-((Dimethylamino)methyl)-4-(trifluoromethoxy)phenol

https://huagongshe.com/reaction/1071214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
Reactantp-(Trifluoromethoxy)phenolHCID 70015—
Product2-((Dimethylamino)methyl)-4-(trifluoromethoxy)phenolHCID 10059958—

Reaction Conditions

Temperature3 °C

Reaction Steps

130 g of 4-trifluoromethoxyphenol are initially charged in 97 ml of 40% aqueous dimethylamine solution and cooled to 3° C. At 0-5° C., 66 ml of 37% aqueous formaldehyde solution are added dropwise within 45 min. The mixture is kept at 5-10° C. for a further 2 hours and is subsequently stirred at room temperature for 19 hours. It is cooled again to 0° C., 4.9 ml of 40% aqueous dimethylamine solution are added and 3.3 ml of 37% aqueous formaldehyde solution are subsequently added dropwise. The mixture is stirred at room temperature for a further 3 hours. The mixture is admixed with 100 ml of water. The organic phase is removed, the aqueous phase is extracted twice with dichloromethane, the combined organic phases are dried and the solvent is distilled off under reduced pressure. The crude product is subsequently fractionally distilled under reduced pressure. 118 g (69% of theory) of a light yellow liquid having a boiling point of 110-112° C. at 18 mbar were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903239B2
Source datasetuspto-grants-2005_06
ORD IDord-3111e731c0144dea8e0a812f295fe090
Source noteuspto-grants-2005_06