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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896986생성일: 2026년 10월 25일

Phenylacetaldehyde → 2-Phenyl-1-(thiophene-2-sulfonylamino)-ethyl-phosphonic Acid Diethyl Ester

https://huagongshe.com/reaction/896986

반응식

참여 물질

역할이름HCID투입량
반응물PhenylacetaldehydeHCID 998—
반응물2-ThiophenesulfonamideHCID 72881—
반응물DiethylphosphiteHCID 3780918—
용매Acetyl chlorideHCID 6367—
생성물2-Phenyl-1-(thiophene-2-sulfonylamino)-ethyl-phosphonic Acid Diethyl EsterHCID 22890932349.4%

반응 조건

온도0 °C

반응 단계

To a suspension of sulfonamide (vi) (500 mg; 0.31 mmol) in acetyl chloride (5 mL) was slowly added diethyl phosphite (400 μL; 0.31 mmol). The reaction was cooled to 0° C. and then phenylacetaldehyde (450 μL; 0.39 mmol) was added dropwise. The reaction was gradually warmed to ambient temperature and after 6 hrs the homogeneous solution was concentrated. The residue was diluted with dichloromethane (25 mL) then washed successively with water (10 mL), saturated sodium bicarbonate (10 mL) and brine (10 mL). The combined organic extracts were dried (MgSO4), evaporated and initially purified by flash chromatography (ethyl acetate-hexanes; 3:2). A second purification by flash chromatography (acetone-hexanes; 3:7) yielded diethyl phosphonate (xii) (437 mg, 35%) as a colorless solid; 1H NMR (400 MHz, CDCl3) δH 1.22 (t, J=7 Hz, 3H, OCH2CH3), 1.26 (t, J=7 Hz, 3H, OCH2CH3), 2.89 (dt, J=8, 14 Hz, 1H, CHPh), 3.12 (dt, J=6, 14 Hz, 1H, CHPh), 3.96-4.23 (m, 5H, NCHP and OCH2CH3), 6.38 (dd, J=2, 9.5 Hz, 1H, NH), 6.92-6.93 (m, 1H, Ar—H), 7.12-7.20 (m, 5H, Ar—H), 7.33-7.34 (m, 1H, Ar—H), 7.43-7.45 (m, 1H, Ar—H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06921756B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-8a87623a2eee4e03aeb1dea61cf47f3e
출처 메모uspto-grants-2005_07