HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1527962Erstellt: 25. Oktober 2026
Acetic Acid → 3-(4-Bromophenyl)-3-o-tolylpropanoic acid
https://huagongshe.com/reaction/1527962
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Ethyl 3-(4-bromophenyl)-2-cyano-3-o-tolylpropanoate | HCID 67015643 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-(4-Bromophenyl)-3-o-tolylpropanoic acid | HCID 67015622 | 21,9% |
Reaktionsschritte
Sulfuric acid (940 g, 9.59 mol) was added over 30 min under ice cooling to a mixture of ethyl 3-(4-bromophenyl)-2-cyano-3-o-tolylpropanoate (200 g, 494 mmol) in acetic acid (1.06 kg, 17.7 mol), while keeping the internal temperature below 27° C., then the reaction mixture was heated at reflux for 20 h. After cooling to 40° C. ice (500 g) and ethyl acetate (1500 mL) were added, the precipitate collected by filtration and washed with water to produce the title compound (34.5 g). The filtrate was partitioned between ethyl acetate and water, the organic layer was washed with brine, dried over magnesium sulfate, filtered, and evaporated. The residue was stored in the refrigerator for 1 h. Then the precipitate was collected by filtration and washed with acetic acid and heptane to afford a second crop of product (96.2 g). Total yield: 130.7 g (83%). Off-white solid, MS: 319.0 [M−H]−.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09090565B2 |
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| Quelldatensatz | uspto-grants-2015_07 |
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| ORD ID | ord-6e7de0c5112c4c35bf703cf39c82d7bd |
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| Quellennotiz | uspto-grants-2015_07 |
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