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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1978854Erstellt: 26. Oktober 2026

Water → 3-[3-(2-Bromo-2-methoxyethoxycarbonylethenyl)-4-chlorophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine

https://huagongshe.com/reaction/1978854

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromoethyl methyl etherHCID 80972—
Edukt3-[3-(2-Bromo-2-carboxyethenyl)-4-chlorophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidineHCID 86583797—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[3-(2-Bromo-2-methoxyethoxycarbonylethenyl)-4-chlorophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidineHCID 86583796—

Reaktionsschritte

0.52 ml of methoxyethyl bromide was added to a solution of 2.27 g of 3-[3-(2-bromo-2-carboxyethenyl)-4-chlorophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine and 0.76 g of potassium carbonate in dimethylformamide, and the resulting solution was stirred for 17 hours. Thereafter, 100 ml of water were added and the aqueous phase was extracted with twice 100 ml of dichloromethane. The combined organic phases were washed with three times 50 ml of water, dried over sodium sulfate and evaporated down. After flash chromatography (dichloromethane→9:1 dichloromethane/ethyl acetate), the title compound was obtained as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06239074B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-114c1d770a8943d2b14aa562839d3948
Quellennotizuspto-grants-2001_05