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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50964Erstellt: 25. Oktober 2026

(2-Chloro-6-nitrophenyl)(3-chloropropyl)sulfane → 3-Chloro-2-[(3-chloropropyl)sulfanyl]aniline

https://huagongshe.com/reaction/50964

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2-Chloro-6-nitrophenyl)(3-chloropropyl)sulfaneHCID 22735865—
LösungsmittelMethanolHCID 887—
Produkt3-Chloro-2-[(3-chloropropyl)sulfanyl]anilineHCID 2273553793%

Reaktionsschritte

The crude 1-chloro-2-[(3-chloropropyl)sulfanyl]-3-nitrobenzene was dissolved in MeOH (150 mL) and degassed with N2. Palladium hydroxide (1.8 g) was added in four portions to this solution in a Parr appararus. The resulting heterogeneous solution was shaken under hydrogenation conditions (55 psi) at room temp for 18 h. The catalyst was removed via filtration in the same manner as above and the filtrate was concentrated in vacuo. to afford 3-chloro-2-[(3-chloropropyl)sulfanyl]aniline (9.94 g, 93%) as a dark oil: 1H NMR (CHCl3, 300 MHz) δ7.03 (t, 1H, J=8.1 Hz), 6.82 (t, 1H, J=8.1 Hz), 6.63 (t, 1H, J=8.0 Hz), 4.62 (br s, 1H), 3.68 (t, 2H, J=6.4 Hz), 2.92 (t, 2H, J=6.9 Hz), 1.98 (quintet, 2H, J=6.6 Hz) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713471B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-904e74b753614e24915791cedb72e393
Quellennotizuspto-grants-2004_03