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HRID 1600533Erstellt: 25. Oktober 2026

Triethylamine → 3,5-dichlorophenyl 2-methyl-2-(6-methyl-5-phenyl-2 3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propionate

https://huagongshe.com/reaction/1600533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3,5-DichlorophenolHCID 11571—
EduktTriphenylphosphineHCID 11776—
Edukt2-methyl-2-(6-methyl-5-phenyl-2,3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propionic acidHCID 22118282—
LösungsmittelCarbon tetrachloride methylene chlorideHCID 22996148—
Produkt3,5-dichlorophenyl 2-methyl-2-(6-methyl-5-phenyl-2 3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propionateHCID 2182989841,8%

Reaktionsschritte

To a suspension of 2-methyl-2-(6-methyl-5-phenyl-2,3-dihydro-4-oxo-4H-1,3-oxazin-3-yl)-propionic acid (1.1 g) in 14 ml of CCl4 --CH2Cl2 (1:1) was added triphenylphosphin (1.38 g), then the mixture was refluxed for 40 min. The reaction mixture was ice-cooled and 3,5-dichlorophenol (0.65 g) and triethylamine (0.4 g) were slowly added, then it was stirred at room temperature for 1 h. After evaporation of the solvent, the residue was dissolved in ethyl acetate. The insolubles were filtered off and the filtrate was evaporated. The residue was purified by chromatography on a silica gel column to get the captioned compound (0.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05977025
Quelldatensatzuspto-grants-1999_11
ORD IDord-bcb15fa2d0de4348bc656e727e5cba34
Quellennotizuspto-grants-1999_11