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HRID 1946847생성일: 2026년 10월 27일

2,5-Dichlorophenol → 4-(2,5-Dichlorophenoxy)-3-nitrobenzonitrile

https://huagongshe.com/reaction/1946847

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DichlorophenolHCID 66—
반응물Potassium CarbonateHCID 11430—
반응물Benzonitrile, 4-chloro-3-nitro-HCID 13655—
용매TetrahydrofuranHCID 8028—
생성물4-(2,5-Dichlorophenoxy)-3-nitrobenzonitrileHCID 5954894281.8%

반응 단계

2,5-Dichlorophenol (17.86 g, 109.54 mmol) and 4-chloro-3-nitrobenzonitrile (10.00 g, 54.77 mmol) were combined with K2CO3 (37.85 g, 273.85 mmol) in THF (300 mL). The reaction mixture was refluxed for 48 hrs and then the solid was filtered over a bed of Celite. After rinsing the residue with copious amounts of DCM, the filtrate was concentrated to produce a yellow solid. The solid was triturated with minimal DCM and collected via vacuum filtration to yield compound 34 (13.84 g, 81.7% yield, 100.0% pure). 1H NMR (500 MHz, DMSO-d6): δ 8.73 (s, 1H), 8.12 (dd, J1=9 Hz, J2=2 Hz, 1H), 7.73 (d, J=9 Hz, 1H), 7.65 (d, J=2 Hz, 1H), 7.48 (dd, J1=9 Hz, J2=2 Hz, 1H), 7.21 (d, J=9 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399456B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-c6845f4a525f42d7a7b4b65c46ef0020
출처 메모uspto-grants-2013_03