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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583472생성일: 2026년 10월 25일

Diethyl (cyanomethyl)phosphonate → 3-(3,4-Diethylphenyl)-3-phenylacrylonitrile

https://huagongshe.com/reaction/583472

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl (cyanomethyl)phosphonateHCID 75676—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물Methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylateHCID 9820154—
반응물3,4-DiethylbenzophenoneHCID 21584598—
용매HexaneHCID 8058—
생성물3-(3,4-Diethylphenyl)-3-phenylacrylonitrileHCID 54306880—

반응 단계

3-(3,4-Diethylphenyl)-3-phenylacrylonitrile was prepared analogously to methyl 3,3-bis-(3,4-dimethoxyphenyl)acrylate using 3,4-diethylbenzophenone (0.95 g, 4 mmol), diethylcyanomethylphosphonate (0.73 mL, 4.4 mmol) and lithium hexamethyldisilazide (3.4 mL, 4.4 mmol, 1.3M) with a reaction time of 2 hours at room temperature. The crude product was purified by flash chromatography (silica gel, 8% ethyl acetate/methylene chloride) to afford an oil which was stirred in hexane until it solidified. The resulting slurry was filtered, the solid washed with hexane, air dried and then dried in vacuo to afford 0.6 g (57%) of a mixture of the E and Z isomers as a white solid: mp 63-64° C.; 1H NMR (CDCl3) δ 7.51-6.99 (m, 16H), 5.72 (s, 2H), 2.76-2.55 (m, 8H), 1.32-1.14 (m, 12H); 13C NMR (CDCl3) δ 163.3, 144.7, 142.2, 137.3, 136.5, 130.2, 129.8, 129.6, 128.6, 128.5, 128.4, 128.3, 127.2, 126.2, 118.2, 93.9, 93.7, 25.5, 25.3, 15.2, 15.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929117
출처 데이터셋uspto-grants-1999_07
ORD IDord-43f248225c464e94bb41b7cab25611fa
출처 메모uspto-grants-1999_07