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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388881생성일: 2026년 10월 27일

Diethyl Ether → 7,7-Dimethyl-5,8-eicosadienoic acid

https://huagongshe.com/reaction/1388881

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Dodecyltriphenylphosphonium bromideHCID 84955—
반응물(Z)-8-Oxo-7,7-dimethyl-5-octenoic acid methyl esterHCID 13276466—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매tetrahydrofuran HMPAHCID 86583969—
생성물7,7-Dimethyl-5,8-eicosadienoic acidHCID 531233149%

반응 조건

온도0 °C

반응 단계

A 1.4 ml. portion of n-butyllithium (1.6 M solution in hexane) was added to a solution of 1.4 g (2.74 mmol) of n-dodecyltriphenylphosphonium bromide in 5.5 ml of 2:1 tetrahydrofuran-hexamethylphosphorictriamide, at -78° C., under argon. The solution turned orange-red in color. To this solution was then added 0.350 g (1.77 mmoles) of (Z)-8-oxo-7,7-dimethyl-5-octenoic acid methyl ester dissolved in 1 ml of tetrahydrofuran, using a syringe. The reaction mixture was stirred for 30 minutes at -78° C. and an additional 45 minutes at 0° C. The product was isolated by ether extraction using the conventional workup procedure and then chromatographed on silica gel. Hexane-ether (19:1) eluted 0.600 g (97%) of (Z,Z)-7,7-dimethyl-5,8-eicosadienoic acid methyl ester. This material was dissolved in 6 ml of methanol and treated with 0.6 ml of 5% aqueous potassium hydroxide. After stirring at room temperature for 17 hours, 3 ml of the methanol was evaporated in vacuo. The remaining solution was acidified with oxalic acid and the product was extracted with ether. The ether extracts were washed with brine, dried over MgSO4 and the solvent evaporated at reduced pressure. Purification of the crude acid on a silica gel column provided 0.292 g (50.7%) of (Z,Z)-7,7-dimethyl-5,8-eicosadienoic acid (ca. 100% pure by GC analysis).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04434101
출처 데이터셋uspto-grants-1984_02
ORD IDord-59ed7aabc2ae4762b22dbab317b0f22e
출처 메모uspto-grants-1984_02