Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Potassium Permanganate | HCID 516875 | — |
| Edukt | 4-(Naphthalene-2-sulphonyl)benzaldehyde | HCID 18357086 | — |
| Katalysator | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(2-Naphthylsulphonyl)benzoic acid | HCID 18357067 | 41,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06313127B1 |
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| Quelldatensatz | uspto-grants-2001_11 |
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| ORD ID | ord-7f0f6e2c1ab046e9bf1dba34cb4817e0 |
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| Quellennotiz | uspto-grants-2001_11 |
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