돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491514생성일: 2026년 10월 26일

1-Iodo-4-nitrobenzene → 1,2-Dichloro-3-(4-nitrobenzyl)benzene

https://huagongshe.com/reaction/491514

반응식

참여 물질

역할이름HCID투입량
반응물1-Iodo-4-nitrobenzeneHCID 12495—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178478089HCID 178478089—
촉매Tris(furan-2-yl)phosphaneHCID 521585—
용매TetrahydrofuranHCID 8028—
생성물1,2-Dichloro-3-(4-nitrobenzyl)benzeneHCID 301737976%

반응 단계

Under an argon stream, bis(dibenzylidenacetone)palladium(0) (3.2 g, 5.6 mmol) and tri(2-furyl)phosphine (2.6 g, 11.2 mmol) were dissolved in THF (310 ml), the reaction mixture of 2,3-dichlorobenzylzinc chloride (421.7 mmol) in THF obtained in Reference Example 1 was added dropwise under ice-cooling through a cannula, and then a solution of 4-iodonitrobenzene (70.0 g, 281 mmol) in THF (700 ml) was added dropwise, after which the mixture was stirred at room temperature for 2 hr, saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was filtered through celite. The filtrate was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure, and the precipitated solid was collected by filtration on the way. The filtrate was again concentrated under reduced pressure, and the precipitated solid was collected by filtration on the way. The collected solids were combined washed with n-hexane and vacuum dried to give the object product (60.2 g, yield 76%) as a pale-brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531554B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-8321250d960f412094fd9c88518effb1
출처 메모uspto-grants-2009_05