HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264778Erstellt: 26. Oktober 2026
1,2-Dichloroethane → Methyl 4-[3-(1-adamantyl)benzoyl]butyrate
https://huagongshe.com/reaction/264778
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1-Chloroadamantane | HCID 64154 | — |
| Edukt | delta-Oxobenzenepentanoic acid | HCID 73914 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Produkt | Methyl 4-[3-(1-adamantyl)benzoyl]butyrate | HCID 19036890 | 24% |
Reaktionsschritte
5.0 g (26.0 mmol) of 4-benzoylbutyric acid was dissolved in 100 ml of 1,2-dichloroethane, and 8.70 g (65.03 mmol) of aluminum trichloride and 5.30 (31.21 mmol) of 1-chloroadamantane were added thereto, followed by stirring the mixture at 60° C. for 6 hours. The reaction mixture was poured into hydrochloric acid, and extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. To the residue were added 100 ml of methanol and 5 ml of conc. sulfuric acid, and the mixture was stirred at room temperature overnight. The solvent was distilled off under reduced pressure, and the residue was poured into water, and extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The resulting residue was purified by silica-gel column chromatography (eluent: a mixture of 1% ethyl acetate and hexane) to obtain 2.13 g of the above-mentioned compound (yield 24%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05646283 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-3f0275be70ee491fa271079bb6395742 |
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| Quellennotiz | uspto-grants-1997_07 |
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