참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Dodecyltriphenylphosphonium bromide | HCID 84955 | — |
| 반응물 | (Z)-8-Oxo-7,7-dimethyl-5-octenoic acid methyl ester | HCID 13276466 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | tetrahydrofuran HMPA | HCID 86583969 | — |
| 생성물 | 7,7-Dimethyl-5,8-eicosadienoic acid | HCID 5312331 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04434101 |
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| 출처 데이터셋 | uspto-grants-1984_02 |
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| ORD ID | ord-59ed7aabc2ae4762b22dbab317b0f22e |
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| 출처 메모 | uspto-grants-1984_02 |
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