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HRID 427435Erstellt: 24. Oktober 2026

Hydrochloric Acid → 4-(2-Naphthylsulphonyl)benzoic acid

https://huagongshe.com/de/reaction/427435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl AcetateHCID 8857—
EduktPotassium PermanganateHCID 516875—
Edukt4-(Naphthalene-2-sulphonyl)benzaldehydeHCID 18357086—
KatalysatorHexadecyltrimethylammonium BromideHCID 5974—
LösungsmittelWaterHCID 962—
Produkt4-(2-Naphthylsulphonyl)benzoic acidHCID 1835706741,1%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

4-(Naphthalene-2-sulphonyl)benzaldehyde (0.97 g) was suspended in water (25 ml) containing cetyltrimethylammonium bromide (58 mg). The mixture was stirred and heated to 60° C., and potassium permanganate (0.95 g) was added in small portions over 1 hour. Heating was continued for a further 2 hours. The mixture was cooled to room temperature and was acidified with 2M hydrochloric acid. Ethyl acetate was added to the stirred mixture, which was filtered through a pad of celite. The ethyl acetate layer was washed with brine, dried (MgSO4), and evaporated to afford 4-(naphthalene-2-sulphonyl)benzoic acid (0.42 g) as solid residue; NMR: 7.7(dd,1H); 7.95(dd,1H), 8.1-8.2(m,8H); 8.7(d,1H); microanalysis, found; C,58.6; H,3.9%; C17H12O4S.2H2O requires: C,58.6; H,4.6%; MS: m/z 312(M H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313127B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-7f0f6e2c1ab046e9bf1dba34cb4817e0
Quellennotizuspto-grants-2001_11