戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1017864作成日:2026年10月27日

Hexane → (1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanol

https://huagongshe.com/reaction/1017864

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
反応物1-Benzyl-4-(4-isopropylbenzoyl)piperidineHCID 21961355—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanolHCID 2196135879.2%

反応手順

To a solution of 2-methoxy-3,4,6-trimethylbromobenzene (15.48 g, 67.56 mmol) in tetrahydrofuran (200 ml), which was kept at −78° C., was added dropwise under an argon atmosphere a solution of n-butyllithium in hexane (1.59 mol/l, 42 ml, 66.78 mmol) and the mixture was stirred for 30 minutes. To this mixture was added dropwise a solution of 1-benzyl-4-(4-isopropylbenzoyl)piperidine (19.81 g, 61.63 mmol) in tetrahydrofuran (50 ml) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extracts were washed with an aqueous saturated solution of sodium chloride, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain 23.01 g (79% yield) of the title compound. Melting point: 154-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479536B1
出典データセットuspto-grants-2002_11
ORD IDord-9de9000d15664affb184365a51e983d8
出典メモuspto-grants-2002_11