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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-(Trifluoromethoxy)phenol | HCID 70015 | — |
| Product | 2-((Dimethylamino)methyl)-4-(trifluoromethoxy)phenol | HCID 10059958 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903239B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-3111e731c0144dea8e0a812f295fe090 |
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| Source note | uspto-grants-2005_06 |
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