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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 575463생성일: 2026년 10월 24일

Potassium Carbonate → (1-((4-Iodo-2-nitrophenoxy)methyl)cyclopropyl)methanol

https://huagongshe.com/ko/reaction/575463

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,1-Bis(hydroxymethyl)cyclopropaneHCID 4101437—
반응물1-Fluoro-4-iodo-2-nitrobenzeneHCID 14590582—
용매DimethylformamideHCID 6228—
생성물(1-((4-Iodo-2-nitrophenoxy)methyl)cyclopropyl)methanolHCID 8669352771%

반응 조건

온도50 °C

반응 단계

A solution of 1-fluoro-4-iodo-2-nitrobenzene (2.50 g, 9.4 mmol) in DMF (30 mL) was treated with 1-(hydroxymethyl)cyclopropylmethanol (1.91 g, 19 mmol) and K2CO3 (2.6 g, 19 mmol) and the mixture was heated at 50° C. for 8 hours. TLC indicated complete consumption of the arylfluoride. The mixture was diluted with water and extracted with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate and concentrated by rotoevaporation. Purification by flash column chromatography (EtOAc in heptanes) gave the titled compound as a light yellow solid (2.31 g, 71% yield). 1H NMR (400 MHz, DMSO) δ 8.15 (d, J=2.2 Hz, 1H), 7.92 (dd, J=8.8, 2.2 Hz, 1H), 7.17 (d, J=8.9 Hz, 1H), 4.60 (t, J=5.6 Hz, 1H), 4.05 (s, 2H), 3.36 (d, J=5.6 Hz, 2H), 0.50 (s, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034866B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-af1aafb3e9064f4bac3bdba56441a578
출처 메모uspto-grants-2015_05