돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50624생성일: 2026년 10월 27일

(4-Fluorophenyl)dimethylphosphine oxide → 1-(Dimethyl-phosphinoyl)-4-nitro-benzene

https://huagongshe.com/reaction/50624

반응식

참여 물질

역할이름HCID투입량
반응물(4-Fluorophenyl)dimethylphosphine oxideHCID 21897903—
반응물HCID 178506934HCID 178506934—
용매IsopropanolHCID 3776—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
용매Sodium chloride; waterHCID 57417360—
생성물1-(Dimethyl-phosphinoyl)-4-nitro-benzeneHCID 2189791245.1%

반응 단계

A sealed pressure flask, flushed with N2, containing a mixture of 3.90 g (22.7 mmol) of 1-(Dimethyl-phosphinoyl)-4-fluoro-benzene and 6.0 g (113.3 mmol) of LiNO2 (for prep see, W. C. Ball and H. H. Abram J. Chem. Soc. 1913, 103, 2130-2134) in 27 mL of DMPU (1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone) was stirred at ambient temperature for 5-10 min (to dissolve fluoro compound) then heated at 190° C. for 3 days. The resulting dark brown solution was cooled to ambient temperature, diluted with 300 mL of brine, then extracted with EtOAc (10×100 mL) until the aqueous layer showed little or no evidence of product by HPLC. The combined organics were dried over MgSO4 and concentrated. The excess DMPU was removed via short-path distillation (120° C./0.3 mm) to provide a semi-solid, which was dissolved in a minimum amount of iPrOH and purified by silica gel flash chromatography (eluted with 5% iPrOH/DCM, then 10% iPrOH/DCM, then 15% iPrOH/DCM) to provide 2.04 g of an yellow solid: 1H NMR (300 MHz, DMSO-d6) δ8.34 (dd, J=8.7, 1.9 Hz, 2H), 8.07 (dd, J=10.6, 8.8 Hz, 2H), 1.75 (s, 3H), 1.70 (s, 3H). 31P NMR (121 MHz, DMSO-d6) δ37.89.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713462B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-bf9184ac45334d598d4f04d6f1e9bb88
출처 메모uspto-grants-2004_03