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HRID 461262作成日:2026年10月26日

Ethylene Glycol → 7-[3-(2-Hydroxyethoxy)-5-oxocyclopent-1-EN-1-YL]heptanoic acid

https://huagongshe.com/reaction/461262

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物2,6-LutidineHCID 7937—
反応物4-Bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-oneHCID 13046277—
触媒Silver tetrafluoroborateHCID 159722—
溶媒WaterHCID 962—
生成物7-[3-(2-Hydroxyethoxy)-5-oxocyclopent-1-EN-1-YL]heptanoic acidHCID 23329941—

反応手順

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 chromatography 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04061672
出典データセットuspto-grants-1977_12
ORD IDord-299c76bb8720488dafe7131c43c1a356
出典メモuspto-grants-1977_12