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HRID 635143作成日:2026年10月27日

2-Hexenoic acid, (2E)- → trans-2-[4-(4-pentylbicyclo[2.2.2]octyl)phenyl]dioxan-5-yl (E)-hex-2-enoate

https://huagongshe.com/reaction/635143

反応式

関与物質

役割名称HCID仕込み量
反応物2-Hexenoic acid, (2E)-HCID 5282707—
反応物1-[4-(trans-5-Hydroxydioxan-2-yl)phenyl]-4-pentylbicyclo[2.2.2]octaneHCID 69963268—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物trans-2-[4-(4-pentylbicyclo[2.2.2]octyl)phenyl]dioxan-5-yl (E)-hex-2-enoateHCID 131722380—

反応条件

温度0 °C

反応手順

A solution of N,N-dicyclohexylcarbodiimide (0.18 g, 0.8 mmol) in dichloromethane (10 cm3) is added to a solution of (E)-hex-2-enoic acid (0.07 g, 0.7 mmol), 1-[4-(trans-5-hydroxydioxan-2-yl) phenyl]-4-pentylbicyclo[2.2.2]octane (0.25 g, 0.7 mmol), 4-(dimethylamino) pyridine (0.04 g) in dichloromethane (20 cm3), cooled in an ice bath (0° C.) under an atmosphere of nitrogen. The reaction mixture is stirred overnight, filtered to remove precipitated material and the filtrate was evaporated down under reduced pressure. The crude product is purified by column chromatography on silica gel using a 9:1 petroleum ether (40-60° C.)/ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield the desired ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06187393B1
出典データセットuspto-grants-2001_02
ORD IDord-79e381452e0a4b0a9549259e1035a63f
出典メモuspto-grants-2001_02