戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 328051作成日:2026年10月26日

Sodium hydride → Cyclopentanecarboxylic acid, 2-hexyl-3-oxo-

https://huagongshe.com/reaction/328051

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Ethyl 2-bromooctanoateHCID 95580—
反応物Ethyl propane-1,1,3-tricarboxylateHCID 86733388—
溶媒DimethylformamideHCID 6228—
溶媒PentaneHCID 8003—
生成物Cyclopentanecarboxylic acid, 2-hexyl-3-oxo-HCID 2057489678%

反応条件

温度25 °C

反応手順

In a 1 L three necked flask fitted with a mechanical stirrer, a thermometer, a nitrogen inlet tube and a calcium chloride drying tube, is placed a suspension of 5.75 g of sodium hydride in 250 ml of dry dimethylformamide. Dry nitrogen is let in and 69 g of ethyl propane-1,1,3-tricarboxylate (G.A. Swan, J.Chem.Sooc., 1039 (1955)) is added dropwise with vigorous stirring. The rate of addition is adjusted to maintain an internal temperature of about 25° C. The reaction mixture is stirred at room temperature until all the sodium hydride has reacted. 60 g of ethyl α-bromocaprylate (K. Bernhard, Helv.Chim.Acta, 29, 1462 (1964)) are added over a period of 1 hour. After the addition has been completed, the reaction mixture is stirred at 100° C for 5 hours. The reaction mixture is cooled to 10° C and added dropwise to a well stirred suspension of 5.75 g of sodium hydride in 50 ml of pentane under nitrogen atmosphere over a period of 2 hours. When the addition is completed, the mixture is stirred at room temperature for an additional 12 hours. The solvent is removed at a reduced pressure and the residue is poured into 1500 ml of cold 5% hydrochloric acid. The organic layer is separated and the water phase is extracted with ether. The combined organic layer and the ether extract are washed with water and sodium carbonate solution and dried over anhydrous sodium sulphate. After removal of the solvent, the unreacted ethyl propane-1,1,3-tricarboxylate is distilled off at 100°-105° C/0,15 mm (16 g) and the residue is boiled for 20 hours with a mixture of 750 ml of acetic acid and 750 ml of concentrated hydrochloric acid. The volatile acids are distilled off at a reduced pressure and the residue is poured onto a large excess of crushed ice. The solid product is collected on a Buchner funnel, washed repeatedly with cold water and dried. The product is recrystallized from cyclohexane-pentane to yield 21,5 g (78%) of 2-n-hexyl-3-oxo-cyclopentane-carboxylic acid melting at 73°-74° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04016109
出典データセットuspto-grants-1977_04
ORD IDord-0cea462cfb76416e9ef3cd6db833ee4a
出典メモuspto-grants-1977_04