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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358097Erstellt: 24. Oktober 2026

Dimethylformamide → 3-Carboethoxymethyl-5-benzylidenerhodanine

https://huagongshe.com/de/reaction/358097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktEthyl BromideHCID 6332—
EduktTetramethylammonium hydroxideHCID 60966—
Edukt(5-Benzylidene-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)acetic acidHCID 2769989—
LösungsmittelMethanolHCID 887—
Produkt3-Carboethoxymethyl-5-benzylidenerhodanineHCID 4340462—

Reaktionsschritte

Under an atmosphere of nitrogen, 4.2 ml of anhydrous N,N-dimethylformamide was added dropwise to 0.279 g of 3-carboxymethyl-5-benzylidenerhodanine (prepared as described in Example 1) at room temperature, and then 1.14 ml of methanol solution of 91.15 mg of tetramethylammonium hydroxide was added dropwise. After the mixture was stirred at room temperature for 20-30 minutes, 0.075 ml of ethyl bromide was added dropwise to the reaction mixture. The mixture was stirred at the same temperature for about 2 hours, and then concentrated under reduced pressure. The residue was diluted with 15 ml of water and extracted with ethyl acetate. The extract was washed with 50 ml of aqueous solution of sodium bicarbonate, 50 ml of water and 50 ml of aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was recrystallized from a mixture of ethyl acetate and n-hexane (1:3) to obtain 14 mg of the titled compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04464382
Quelldatensatzuspto-grants-1984_08
ORD IDord-515fe300fabe4282982376ddf3db2edc
Quellennotizuspto-grants-1984_08