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HRID 1198046Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2,2-dimethyl-3-oxo-N-(2,4,6-trimethoxyphenyl)-tetradecanamide

https://huagongshe.com/reaction/1198046

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2,4,6-TrimethoxyanilineHCID 84271—
Edukt2,2-Dimethyl-3-oxo-tetradecanoic acid ethyl esterHCID 10063293—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelBenzeneHCID 241—
Produkt2,2-dimethyl-3-oxo-N-(2,4,6-trimethoxyphenyl)-tetradecanamideHCID 1004861526%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a flask containing 10 mL benzene which had been flushed with nitrogen, trimethylaluminum (2.0M hexane solution, 0.003 mol, 1.14 eq) was added dropwise and cooled to 5° C. A solution of 2,4,6-trimethoxyaniline (0.653 g, 0.003 mol) in 1.5 mL benzene was added dropwise (exotherm to 10° C.) and stirred for 20 minutes at 5° C. The ice bath was removed and the contents were allowed to gradually warm to room temperature over a 45-minute period. A solution of 2,2-dimethyl-3-oxo-tetradecanoic acid ethyl ester (1.0 g, 0.003 mol) in 1.5 mL benzene was added dropwise and the resulting reaction mixture was heated to reflux for 16 hours (M. F. Lipton, et al, Org. Syn. Coll. Vol. 2, 492). After cooling to room temperature, the mixture was hydrolyzed slowly with 2% HCl solution (5 mi) and stirred for 20 minutes. The layers were then separated and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried (MgSO4), and concentrated in vacuo (30° C.) to yield a residue which was washed with hot hexanes, cooled, filtered, and oven-dried to yield 0.340 g (0.78 mmol, 26%) of the title compound, mp 92°-94° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05278326
Quelldatensatzuspto-grants-1994_01
ORD IDord-64fb43b553ec4509999e44df3ba2e163
Quellennotizuspto-grants-1994_01