HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2384316Erstellt: 25. Oktober 2026
2-Amino-4-chlorophenol → N-(5-Chloro-2-hydroxyphenyl)-3,5-dichlorobenzamide
https://huagongshe.com/reaction/2384316
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Amino-4-chlorophenol | HCID 7265 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3,5-Dichlorobenzoyl chloride | HCID 76191 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-(5-Chloro-2-hydroxyphenyl)-3,5-dichlorobenzamide | HCID 17860185 | 32,4% |
Reaktionsschritte
2-Amino-4-chlorophenol (316 mg, 2.2 mmol) and triethylamine (243 mg, 2.4 mmol) were dissolved in dichloromethane (5 mL). A solution of 3,5-dichlorobenzoyl chloride (419 mg, 2 mmol) in dichloromethane (2 mL) was added dropwise under ice cooling and argon atmosphere, and the mixture was stirred at room temperature for 15 hours. After the reaction mixture was diluted with ethyl acetate, washed with water and brine one after another, dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give a light brown solid. The solid was suspended and washed with n-hexane-ethyl acetate under heating at reflux to give the title compound (205 mg, 32.4%) as a white crystal.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08263657B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-e20f65288f2848c1928d81c74a7e9963 |
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| Quellennotiz | uspto-grants-2012_09 |
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