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HRID 264778作成日:2026年10月27日

1,2-Dichloroethane → Methyl 4-[3-(1-adamantyl)benzoyl]butyrate

https://huagongshe.com/reaction/264778

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物Hydrochloric AcidHCID 313—
反応物1-ChloroadamantaneHCID 64154—
反応物delta-Oxobenzenepentanoic acidHCID 73914—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物Methyl 4-[3-(1-adamantyl)benzoyl]butyrateHCID 1903689024%

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646283
出典データセットuspto-grants-1997_07
ORD IDord-3f0275be70ee491fa271079bb6395742
出典メモuspto-grants-1997_07