Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Edukt | 2-Methyl-3-nitrophenol | HCID 79579 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-Chloro-2-methyl-3-nitrophenol | HCID 18789636 | — |
Reaktionsschritte
2-Methyl-3-nitrophenol (25.5 g), N-chlorosuccinimide (44.5 g), and trifluormethanesulfonic acid (50.0 g) were combined in dry acetonitrile (500 mL) and allowed to stir under an atmosphere of nitrogen at 75° C. for 1.5 hr. The reaction mixture was cooled to room temperature, diluted with ethyl ether (650 mL), washed with water, 10% sodium bisulfite solution, water, and finally saturated sodium chloride solution. Evaporation of the solvent afforded a crude material which was flash chromatographed on silica and eluted with acetone:hexane (1:9) to afford 16.8 g as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05952362 |
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| Quelldatensatz | uspto-grants-1999_09 |
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| ORD ID | ord-254b63ae05a547bdbb40d5d13db1ee86 |
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| Quellennotiz | uspto-grants-1999_09 |
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