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HRID 1464523作成日:2026年10月27日

p-Toluenesulfonic acid → 5-(2,3,4,5-Tetramethoxy-6-methylphenyl)-5-phenylpentane-1-ol

https://huagongshe.com/reaction/1464523

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-Chloro-1-butanolHCID 13569—
反応物2,3-Butanediamione, 2,3-dimethyl-HCID 123390—
反応物Tetrahydropyranyl etherHCID 263182—
反応物Sodium BicarbonateHCID 516892—
反応物1-Benzyl-2,3,4,5-tetramethoxy-6-methylbenzeneHCID 19088028—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-(2,3,4,5-Tetramethoxy-6-methylphenyl)-5-phenylpentane-1-olHCID 1908807269%

反応手順

A 3.1 ml (5.0 mmole) of n-butyllithium.hexane solution was added dropwise to 1.51 g (5.0 mmole) of 1-benzyl-2,3,4,5-tetramethoxy-6-methylbenzene and 0.83 ml (5×1.1 mmole) of 1,1,2,2-tetramethylethylenediamine dissolved in anhydrous tetrahydrofuran (15 ml), under an atmosphere of argon at -5° C. over the period of 5 minutes, followed by stirring at -5° to 0° C. for 25 minutes. Then, a solution of 0.96 g (5.0 mmole) of 4-chlorobutanol.tetrahydropyranyl ether in tetrahydrofuran (5 ml) was added to the mixed solution over the period of 5 minutes, followed by stirring for further 15 minutes under ice-cooling. Subsequently, the cooling bath was removed, and stirring was effected at room temperature for 20 minutes. The reaction solution was cooled with ice, and made acid by adding a 10% aqueous phosphoric acid solution, and the product was extracted with isopropyl ether. The organic layer was separated out, washed with aqueous sodium chloride solution, dried (magnesium sulfate). The solvent was distilled off and the residue was dissolved in methanol (15 ml), followed by addition of 48 mg (5×1/20 mmole) of p-toluenesulfonic acid and stirring at 70° C. for 15 minutes. After cooling by standing at room temperature, the mixed solution was neutralized by adding an aqueous sodium hydrogen-carbonate solution, and the solvent was distilled off. Isopropyl ether and water were added to the residue to effect extraction. The isopropyl ether layer was washed with aqueous sodium chloride solution, dried (magnesium sulfate) and evaporated. The residual solution was chromatographed on a silica gel column to perform purification (elution with isopropyl ether) to thereby give 1.29 g (69%) of 5-(2,3,4,5-tetramethoxy-6-methylphenyl)-5-phenylpentane-1-ol. Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 14.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05304658
出典データセットuspto-grants-1994_04
ORD IDord-697b50deb7f249699e158028c10d63ce
出典メモuspto-grants-1994_04