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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65233생성일: 2026년 10월 24일

p-Bromochlorobenzene → 1-Chloro-4-(2-propyn-1-yl)benzene

https://huagongshe.com/ko/reaction/65233

반응식

참여 물질

역할이름HCID투입량
반응물p-BromochlorobenzeneHCID 7806—
반응물Ammonium ChlorideHCID 25517—
반응물1-Methoxypropa-1,2-dieneHCID 139403—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매N-[4-(1-Hydroxy-2-(1H-imidazol-1-yl)ethyl]phenyl]methanesulfonamideHCID 13763390—
생성물1-Chloro-4-(2-propyn-1-yl)benzeneHCID 13660255—

반응 단계

In a flask containing 59 g (2.43 mole) magnesium turnings in 500 ml anhydrous ether under an atmosphere of nitroge add slowly a solution of 465 g (2.43 mole) of 4-bromochlorobenzene in 1 liter 4 anhydrous ether. With caution, once the Grignard has started maintain slow reflux until all 4-bromochlorobenzene has been added. Stir an additional hour and then add this Grignard (maintain slow reflux) to a suspension of 170 g (2.43 mole) methoxyallene and 69 g of cuprous bromide in 300 ml anhydrous ether under N2. When addition is complete, stir another 10 minutes and then add saturated ammonium chloride. Decant off the ether solution wash the solid residue with ether (3×50 ml). Combine the ether extracts and wash with 1N HCl, saturated aqueous sodium bicarbonate, water and dry over magnesium sulfate. Evaporate off the ether and distill the residue in vacuo to obtain the title compound (99-105mmHg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04613609
출처 데이터셋uspto-grants-1986_09
ORD IDord-1d42ee52890f4ac9a7be41fcf2c87f49
출처 메모uspto-grants-1986_09