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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67137생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물GlycerolHCID 753—
반응물4-AcetylbiphenylHCID 7113—
반응물Ethyl bromoacetateHCID 7748—
반응물Ammonium HydroxideHCID 14923—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
용매Trimethyl borateHCID 8470—
생성물3-(4-Biphenylyl)-2-butenoic acid ethyl esterHCID 54501672—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04344966
출처 데이터셋uspto-grants-1982_08
ORD IDord-22a95e6c2cb74ed18706d6a6ec9e84cd
출처 메모uspto-grants-1982_08