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HRID 231006作成日:2026年10月26日

Hydrochloric Acid → 4'-Methoxy-4-(2-methylbutyryl)biphenyl

https://huagongshe.com/reaction/231006

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-MethoxybiphenylHCID 11943—
反応物Butanoyl chloride, 2-methyl-HCID 93697—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒DichloromethaneHCID 6344—
生成物4'-Methoxy-4-(2-methylbutyryl)biphenylHCID 1511394248%

反応条件

温度0 °C

反応手順

A solution of 0.15 mole(15.0 g) of (S)-(+)-2-methylbutyric acid and 0.3 mole(35.5 g) of thionyl chloride in 100 ml of chloroform was refluxed for three hours. After chloroform and the excessive thionyl chloride had been distilled out at reduced pressure, the reaction solution was concentrated at reduced pressure to obtain 12.8 g of 2-methylbutyryl chloride. A suspension of 0.1 mole(13.3 g) of aluminium chloride in 100 ml of dry methylene chloride was cooled to 0° C., then 12.8 g of 2-methylbutyryl chloride was added dropwise thereto, and stirred for 30 min. Maintaining the mixed solution at 0° C., a solution of 0.08 mole(14.7 g) of 4-methoxybiphenyl in 80 ml of dry methylene chloride was added dropwise, and stirred for 10 hours at room temperature. The reaction mixture was decomposed by adding into ice and dil. hydrochloric acid, and the organic layer was washed with dil. hydrochloric acid and an aquious sodium hydrogen carbonate solution, and then dried with magnesium sulfate. The concentrated product was purified by column chromatography to obtain 10.3 g of 4'-methoxy-4-(2-methylbutyryl)biphenyl. (yield: 48%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04844835
出典データセットuspto-grants-1989_07
ORD IDord-e29a2677c30e40518e2249eec0c8eb61
出典メモuspto-grants-1989_07