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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831618Generated: October 31, 2026

2,4,6-Trimethylaniline → HCID 21912272, compound

https://huagongshe.com/reaction/1831618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylanilineHCID 6913—
ReactantHCID 21912249HCID 21912249—
ProductHCID 21912272HCID 21912272—

Reaction Steps

A mixture of butyl-(6-chloro-2-methyl-pyrimidin-4-yl)-ethylamine (1.006 g, 4.42 mmol), and 2,4,6-trimethylaniline (3 ml) was heated at reflux overnight. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated to give 2.862 g of a brown oil. The oil was purified through silica gel column chromatography to give 981 mg (68%) of title compound as a yellow oil. 1H NMR (CDCl3) δ 0.80 (t, 3H), 1.1–1.3 (m, 2H), 1.3–1.5 (m, 2H), 2.17 (s, 6H), 2.27 (s, 3H), 2.41 (s, 3H), 3.2 (m, 2H), 3.36 (m, 2H), 4.66 (s, 1H), 6.90 (s, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067664B1
Source datasetuspto-grants-2006_06
ORD IDord-baefc19e912848919bd3a1fdc8518bb9
Source noteuspto-grants-2006_06