참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | 2,6-Lutidine | HCID 7937 | — |
| 반응물 | 4-Bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one | HCID 13046277 | — |
| 촉매 | Silver tetrafluoroborate | HCID 159722 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 7-[3-(2-Hydroxyethoxy)-5-oxocyclopent-1-EN-1-YL]heptanoic acid | HCID 23329941 | — |
반응 단계
To a stirred solution of 19.1 g. of crude 4-bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one (Example 93) in 310 ml. of ethylene glycol is added 15.6 g. (80 mmole) of silver fluoborate during 2 minutes. The exothermic reaction is controlled to give a temperature of 29° C., and after 1 minute the mixture is treated during 1 minute with 8.6 g. (80 mmole) of 2,6-lutidine. The mixture is stirred at ambient temperature for 2 hours, diluted with water, and filtered. The filtrate is diluted with saturated sodium chloride solution and extracted with ether. The extract is washed with half-saturated sodium chloride solution containing a little hydrochloric acid and saturated sodium chloride solution. The extract is dried over magnesium sulfate and concentrated. Column chromatograph of the residue on silica gel gives an oil, λ maxMeOH = 216 mμ (8350); ν max = 3340 (hydroxyl groups), 1700 (carbonyl groups), and 1620 cm -1 (olefin group).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE029469 |
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| 출처 데이터셋 | uspto-grants-1977_11 |
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| ORD ID | ord-4e33cb807c654094920a24a08568b85c |
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| 출처 메모 | uspto-grants-1977_11 |
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