돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1416101생성일: 2026년 10월 27일

Iodine → 1,1-Di(p-tolyl)ethylene

https://huagongshe.com/reaction/1416101

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 13776575.7%

반응 단계

Into a 1-liter reaction flask were introduced in a nitrogen stream 15.6 g (0.65 mol) of magnesium and 20 ml of THF. Slight amounts of ethyl iodide and iodine were added thereto to initiate reaction. A solution of 111.15 g (0.65 mol) of p-bromotoluene in 500 ml of THF was then added dropwise at room temperature to 40° C. over a period of 2 hours to prepare a Grignard reagent. Thereto was added dropwise a solution of 83.75 g (0.625 mol) of p-methylacetophenone (10a) in 200 ml of THF at that temperature over a period of 3 hours. This mixture was stirred first at room temperature for 3 hours and then with refluxing for 4 hours. The resulting reaction mixture was cooled and poured into 1 liter of 5% aqueous sulfuric acid solution to conduct hydrolysis. This mixture was extracted with toluene, and the extract was washed with aqueous soda ash solution and then with water and concentrated. Thereto were added 300 ml of toluene and 0.5 g of PTSA. The resulting mixture was stirred with refluxing for 4 hours to conduct azeotropic dehydration, followed by washing with aqueous soda ash solution, washing with water, and concentration. The resulting crude 1,1-di(p-tolyl)ethylene (9b) was distilled with a Claisen flask equipped with a vigreux, giving 98.5 g of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05910610
출처 데이터셋uspto-grants-1999_06
ORD IDord-02cb3a42deb540e19464722a5769f95f
출처 메모uspto-grants-1999_06