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HRID 616144Erstellt: 25. Oktober 2026

Dimethylformamide → 2-Nitro-4-[(2,2,3,3-tetrafluoropropyl)sulfanyl]aniline

https://huagongshe.com/reaction/616144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt4-Amino-3-nitrophenyl thiocyanateHCID 104677—
Edukt1,1,2,2-Tetrafluoro-3-iodopropaneHCID 542861—
EduktSodium borohydrideHCID 4311764—
LösungsmittelWaterHCID 962—
Produkt2-Nitro-4-[(2,2,3,3-tetrafluoropropyl)sulfanyl]anilineHCID 20371139—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5 G. of 1-amino-2-nitro-4-thiocyanatobenzene in 20 ml. of dimethylformamide is treated under nitrogen with 0.97 g. of sodium borohydride in 10 ml. of dimethylformamide at 20°-30° C. After 1 hour at 20°-25° C, 6 g. of 2,2,3,3-tetrafluoro-1-iodopropane is added and the mixture is heated at 100° C for 4 hours. The mixture is cooled, diluted with water and extracted with chloroform. Evaporation of the dried chloroform solution yields 2-nitro-4-(2,2,3,3-tetrafluoropropylthio)aniline as an oil. Acetylation of the latter compound in acetic anhydride with sulfuric acid catalysis according to the first paragraph of Example XXI yields 1-acetamido-2-nitro-4-(2,2,3,3-tetrafluoropropylthio)benzene which can be isolated by extraction into chloroform. Alternatively, this may be prepared by substituting 1-acetamido-2-nitro-4-thiocyanatobenzene in the above alkylation reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04072696
Quelldatensatzuspto-grants-1978_02
ORD IDord-ca1c6016dd634a4183a0cf3a63eabbb7
Quellennotizuspto-grants-1978_02