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HRID 15694作成日:2026年10月25日

Toluene → 1-(2-Methyl-1,3-dioxolan-2-yl)-2-(1-hydroxy-2,3,4,5-tetramethyl-2-cyclopentenyl)benzene

https://huagongshe.com/reaction/15694

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2,3,4,5-Tetramethyl-2-cyclopentenoneHCID 41092—
反応物2-(2-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 615284—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-(2-Methyl-1,3-dioxolan-2-yl)-2-(1-hydroxy-2,3,4,5-tetramethyl-2-cyclopentenyl)benzeneHCID 2301622535.1%

反応条件

温度25 °C

反応手順

Under a nitrogen atmosphere, a solution of 2-(2-methyl-1,3-dioxolan-2-yl)-bromobenzene (1.22 g, 5.0 mmol) in tetrahydrofuran (7.3 g) was cooled to −10° C. and a solution of n-butyllithium in n-hexane (1.56 M, 3.4 mL) was added dropwise thereto. After keeping the temperature for 1 hr, a solution of 2,3,4,5-tetramethylcyclopentenone (0.73 g, 5.3 mmol) in tetrahydrofuran (4.9 g) was added dropwise to the mixture. After raising the temperature to 25° C., the mixture was stirred for 3 hrs. After quenching the reaction by addition of toluene and water, the aqueous layer was removed. The obtained organic layer was washed with saturated brine and then dried over sodium sulfate, and the solvent was removed. After concentration, the residue was washed with cooled hexane to give 1-(2-methyl-1,3-dioxolan-2-yl)-2-(1-hydroxy-2,3,4,5-tetramethyl-2-cyclopentenyl)benzene (0.53 g, yield 35.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732643B2
出典データセットuspto-grants-2010_06
ORD IDord-39da437e9a8f4fa7a9c615c95176064a
出典メモuspto-grants-2010_06