関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 1-Chloroadamantane | HCID 64154 | — |
| 反応物 | delta-Oxobenzenepentanoic acid | HCID 73914 | — |
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 生成物 | Methyl 4-[3-(1-adamantyl)benzoyl]butyrate | HCID 19036890 | 24% |
反応手順
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%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05646283 |
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| 出典データセット | uspto-grants-1997_07 |
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| ORD ID | ord-3f0275be70ee491fa271079bb6395742 |
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| 出典メモ | uspto-grants-1997_07 |
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