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HRID 1646818作成日:2026年10月27日

Phosphoric Acid → 7-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-7-phenylheptane

https://huagongshe.com/reaction/1646818

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物1-BromohexaneHCID 8101—
反応物2,3-Butanediamione, 2,3-dimethyl-HCID 123390—
反応物1-Benzyl-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 19088020—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物7-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-7-phenylheptaneHCID 1908808277.3%

反応手順

A 3.1 ml (5.0 mmole) portion of n-butyllithium.hexane solution was added dropwise to 1.35 g (5.0 mmole) of 1-benzyl-2,5-dimethoxy-3,4,6-trimethylbenzene 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 50° C. over the period of 5 miniutes, followed by stirring at 50° to 55° C. for 25 minutes. Then, a solution of 0.83 g (5.0 mmole) of n-hexyl bromide in tetrahydrofuran (5 ml) was added dropwise to the mixed solution over the period of 5 minutes, followed by stirring at 50° C. for further 10 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) and evaporated. The residual solution was chromatographed on a silica gel column to effect purification (elution with hexane/isopropyl ether) to thereby give 1.37 g (77%) of 7-(2,5-dimethoxy-3,4,6-trimethylphenyl)-7-phenylheptane. Its typical physical properties and nuclear magnetic resonance specrum data are shown in Table 14.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05180742
出典データセットuspto-grants-1993_01
ORD IDord-b0f07b3ee53f4fe5b8a5864654260314
出典メモuspto-grants-1993_01