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HRID 1597736생성일: 2026년 10월 26일

Iodine → 1,1-Di(p-tolyl)ethylene

https://huagongshe.com/reaction/1597736

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sulfuric AcidHCID 1118—
반응물IodoethaneHCID 6340—
반응물4-BromotolueneHCID 7805—
반응물p-METHYLACETOPHENONEHCID 8500—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물1,1-Di(p-tolyl)ethyleneHCID 137765—

반응 단계

15.6 g (0.65 mol) of magnesium and 20 ml of THF were placed in a 1-liter reaction flask in a stream of nitrogen, the reaction was initiated with a small amount of ethyl iodide and iodine, and a solution of 111.15 g (0.65 mol) of p-bromotoluene in 500 ml of THF was added dropwise at a temperature from room temperature to 40° C. for 2 hours to prepare a Grignard reagent. A solution of 83.75 g (0.625 mol) of p-methylacetophenone (11c) in 200 ml of THF was added dropwise thereto at the same temperature for 3 hours. The resulting solution was stirred at room temperature for 3 hours, and subsequently stirred under reflux for 4 hours. Then, the solution was cooled, and poured into 1 liter of 5% aqueous sulfuric acid to conduct hydrolysis. The resulting product was extracted with toluene, and the extract was washed with aqueous soda ash, washed with water, and concentrated. Then, 300 ml of toluene and 0.5 g of PTSA were added thereto, followed by stirring under reflux for 4 hours to carry out azeotropic dehydration. The resulting product was washed with aqueous soda ash, washed with water, and concentrated. Crude 1,1-di(p-tolyl)ethylene (9c) was distilled in a Claisen flask equipped with a vigreux to obtain 98.5 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05736284
출처 데이터셋uspto-grants-1998_04
ORD IDord-f3012dea11b54feba994cbfa04ab3b5d
출처 메모uspto-grants-1998_04