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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 511214생성일: 2026년 10월 27일

Chlorodimethylphosphine → Dimethyl(3-nitrobenzyl)phosphane oxide

https://huagongshe.com/reaction/511214

반응식

참여 물질

역할이름HCID투입량
반응물ChlorodimethylphosphineHCID 69936—
반응물Benzene, 1-(bromomethyl)-3-nitro-HCID 77568—
반응물Sodium ethoxideHCID 2723922—
용매TetrahydrofuranHCID 8028—
생성물Dimethyl(3-nitrobenzyl)phosphane oxideHCID 6725632928%

반응 단계

A solution of chlorodimethylphosphine (250 mg, 2.60 mmol) in THF (0.7 mL) was added dropwise to a stirred suspension of sodium ethoxide (194 mg, 2.85 mmol) in THF (0.8 mL) at 0° C. The resulting mixture was stirred at room temperature for 30 min. then treated with 1-(bromomethyl)-3-nitrobenzene (560 mg, 2.59 mmol). The mixture was then stirred under nitrogen at 100° C. in a sealed tube for 2 h., concentrated in vacuo and the residue purified by chromatography over silica gel eluting with 5% MeOH in dichloromethane to afford 153 mg of dimethyl(3-nitrobenzyl)phosphane oxide (yield: 28%). 1H-NMR (CDCl3, 400 MHz): δ=1.53 (d, J=12.4 Hz, 6 H), 3.27 (d, J=14.0 Hz, 2 H), 7.55 (t, J=7.6 Hz, 1 H), 7.71 (d, J=7.6 Hz, 1 H), 8.11 (d, J=2.0 Hz, 1 H), 8.16 (dd, J=0.8, 7.2 Hz, 1 H). MS (ES+): m/z 214.00 (MH+). HPLC: tR=2.16 min (ZQ3, polar—5 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096624B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-01462e2659b644d098059711fc17343f
출처 메모uspto-grants-2015_08