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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1464522생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1464522

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물1-BromohexaneHCID 8101—
반응물2,3-Butanediamione, 2,3-dimethyl-HCID 123390—
반응물1-Benzyl-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 19088020—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물7-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-7-phenylheptaneHCID 1908808277%

반응 단계

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 minutes, followed by stirring at 50° to 55° C. for 25 minutes. Then, a solution of 0.83 (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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05304658
출처 데이터셋uspto-grants-1994_04
ORD IDord-be66aef433ea4838aa4ef1014b7dc05c
출처 메모uspto-grants-1994_04