戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 67137作成日:2026年10月24日

Glycerol → 3-(4-Biphenylyl)-2-butenoic acid ethyl ester

https://huagongshe.com/ja/reaction/67137

反応式

関与物質

役割名称HCID仕込み量
反応物GlycerolHCID 753—
反応物4-AcetylbiphenylHCID 7113—
反応物Ethyl bromoacetateHCID 7748—
反応物Ammonium HydroxideHCID 14923—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
溶媒Trimethyl borateHCID 8470—
生成物3-(4-Biphenylyl)-2-butenoic acid ethyl esterHCID 54501672—

反応手順

6.45 g (0.1 mole) of activated zinc metal (20 mesh) is placed in a flask fitted with a septum inlet and a magnetic stirrer. The system is maintained under a nitrogen atmosphere and kept at a temperature of 25° C. on a water bath. A solution of 19.6 g (0.1 mole) of 4-acetylbiphenyl in 75 ml of dry tetrahydrofuran and 75 ml of trimethyl borate (distilled from calcium hydride) is injected and the mixture stirred. 11.1 ml (0.1 mole) of freshly distilled ethyl bromoacetate is injected in one shot and the mixture stirred at 25° C. for 12 hours. A mixture of 25 ml of concentrated ammonium hydroxide and 75 ml of glycerine is added, and the aqueous phase is separated and extracted thrice with 25 ml portions of diethyl ether. The combined organic extracts are dried over anhydrous magnesium sulphate and the diethylether removed on a rotary evaporator, the residue is vacuum distilled and the fraction distilling at 0.125 mn at 171°-172° C. is collected. Recrystallisation from petroleum ether yields the heading compound, substantially in trans form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04344966
出典データセットuspto-grants-1982_08
ORD IDord-22a95e6c2cb74ed18706d6a6ec9e84cd
出典メモuspto-grants-1982_08