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HRID 234270作成日:2026年10月26日

Isobutyrophenone → 1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanol

https://huagongshe.com/reaction/234270

反応式

関与物質

役割名称HCID仕込み量
反応物IsobutyrophenoneHCID 69144—
反応物2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanolHCID 1054211180.2%

反応手順

A solution of 2-bromo-3,5,6-trimethylanisole (3.0 g, 13.1 mmol) in tetrahydrofuran (20 ml) was cooled to -78° C. and n-butyllithium (1.6M solution in hexane, 8.2 ml, 13.1 mmol) was added dropwise. The reaction mixture was stirred at the same temperature for 15 minutes. Then a solution of isobutyrylbenzene (1.94 g, 13.1 mmol) in tetrahydrofuran (5 ml) was added dropwise and the resulting mixture was stirred at room temperature for additional 30 minutes. The reaction mixture was diluted with water and the product was extracted with isopropyl ether. The extract was washed with water, dried and then concentrated. The residue was crystallized from hexane to obtain the desired compound (3.13 g, yield: 80.2%), m.p. 80°-81° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594154
出典データセットuspto-grants-1997_01
ORD IDord-0e405f99f24a454c906ef7056abc014c
出典メモuspto-grants-1997_01