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HRID 1519255Erstellt: 25. Oktober 2026

Diethyl dithiophosphate, potassium salt → 2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1519255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl dithiophosphate, potassium saltHCID 1385274—
Edukt4-Cyano-2'-nitro-biphenyl-2-carboxylic acid methyl esterHCID 86679831—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl esterHCID 8667983252%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

O,O′-Diethyl dithiophosphate (available from Aldrich Chemical Company, Inc.; 6.85 g, 36.8 mmol) was added to a solution of compound 4-cyano-2′-nitro-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 3; 8.62 g, 30.5 mmol) in a mixture of THF (96 mL) and water (24 mL). The resulting mixture was stirred at 80° C. for 45 h and then evaporated to a small volume. Ethyl acetate (500 mL) was added and the mixture was washed with water (250 mL) and sat. NaHCO3 (250 mL), dried over anhydrous sodium sulfate, filtered, evaporated, and purified by silica gel chromatography, using 17-50% ethyl acetate/petroleum ether as eluent, to give 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (5.0 g, 52%). 1H NMR (300 MHz, CDCl3) δ 8.50 (d, J=2.1 Hz, 1H), 8.18-8.15 (m, 2H), 7.70-7.54 (m, 3H), 7.32 (s, 1H), 7.30 (s, 1H), 7.24 (d, J=1.2 Hz, 1H), 3.69 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09073881B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-f807f09ddd5143e3810c0ecbe0c00424
Quellennotizuspto-grants-2015_07