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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611726Generated: November 2, 2026

Dimethylamine → HCID 22255910, compound

https://huagongshe.com/reaction/1611726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant2,4-Di-tert-butylphenolHCID 7311—
Reactant3,4-DimethylbenzaldehydeHCID 22278—
SolventWaterHCID 962—
ProductHCID 22255910HCID 2225591059%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 26.82 g (0.13 mol) of 2,4-di-tert-butylphenol, 17.44 g (0.13 mol) of 3,4-di-methylbenzaldehyde and 22.0 g (0.20 mol) of a 40% aqueous solution of dimethylamine is heated in a closed vessel at 140° C. for 10 hours, the internal pressure rising to 4 bar. After cooling to room temperature, the reaction mixture is poured into 100 ml of water and extracted twice using ethyl acetate. The organic phases are combined, dried over sodium sulfate and concentrated using a vacuum rotary evaporator. Crystallisation of the residue from isopropanol yields 28.25 g (59%) of 2,4-di-tert-butyl-6-[dimethylamino-(3,4-dimethyl-phenyl)-methyl]-phenol, m.p. 82-85° C., (compound (201), Table 2). Molecular weight C25H37NO (367.58). Analysis, calculated: C 81.69; H 10.15; N 3.81%. Analysis, found: C 81.78; H 10.05; N 3.80%. 1HNMR (300 MHz, CDCl3, ppm): 1.18 (s, 9H); 1.43 (s, 9H); 2.21 (s, 6H); 2.24 (s, 6H); 4.27 (s, 1H); 6.74 (d, 1H); 7.11 (m, 4H); 12.43 (s, 1H

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989446B2
Source datasetuspto-grants-2006_01
ORD IDord-8d86b26e1e55412fb9747df9e2f79a22
Source noteuspto-grants-2006_01