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HRID 23614Erstellt: 24. Oktober 2026

Acetic Acid → Diethyl 2-{[(4-methylthien-3-yl)amino]methylene}malonate

https://huagongshe.com/de/reaction/23614

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDiethyl (ethoxymethylene)malonateHCID 6871—
EduktSodium HydroxideHCID 14798—
EduktMethyl 3-amino-4-methylthiophene-2-carboxylateHCID 123584—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktDiethyl 2-{[(4-methylthien-3-yl)amino]methylene}malonateHCID 2807959—

Reaktionsschritte

To a solution of methyl 3-amino-4-methylthiophene-2-carboxylate (commercially available from Avocado, catalog number 10115, 5.00 g, 29.2 mmol) in 95% ethanol (25 mL) was added 1.0 N NaOH (35 mL). The mixture was heated to reflux and stirred for 2.5 hrs. The resulting solution was cooled to room temperature before the addition of glacial acetic acid (2.05 mL, 35.8 mmol). After stirring for 5 minutes at room temperature, diethyl ethoxymethylenemalonate (DEEM, 6.5 mL, 32.2 mmol) was added. The mixture was stirred vigorously until it nearly solidified (ca. 5 min), and then it was left standing at room temp for 3 hours. 95% ethanol (60 mL) was added, and the mixture was warmed on a steam bath until solution was achieved. Water (50 mL) was added with continued heating on the steam bath, resulting in a slightly cloudy solution. The flask was removed from the steam bath and allowed to cool to room temp and then placed in a 0° C. refrigerator, at which point crystallization of the product as fine white filaments was rapid. After standing at 0° C. for. 2 hours, the mixture was filtered. The collected solid was washed with 50% ethanol/water and dried, affording a white solid (5.79 g). The filtrate was diluted with water to a total volume of 500 mL, left overnight at 0° C., and filtered to afford a second crop (0.96 g) that was of equal purity to the first crop by HPLC analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-18cad0b4d8a44beb9089ffca030accd4
Quellennotizuspto-grants-2005_02