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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 418891생성일: 2026년 10월 26일

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetate

https://huagongshe.com/reaction/418891

반응식

참여 물질

역할이름HCID투입량
반응물Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
반응물2-(3-Methoxyphenyl)cyclohexanoneHCID 85868—
용매TolueneHCID 1140—
생성물Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetateHCID 5372010899.8%

반응 단계

Combine 2-(3-methoxyphenyl)-cyclohexanone (5.0 g, 24.5 mmol), carbethoxymethylene triphenylphosphorane (15.4 g, 44.1 mmol), and toluene (150 mL), stir and heat at reflux. After 22 hours, cool to ambient temperature and concentrate under vacuum. Add ether and filter off the triphenylphosphine oxide precipitate and concentrate the ether filtrate. Flash chromatograph with 0% to 10% ethyl acetate/hexanes to yield the titled compound (6.71 g, 99%) as a clear oil. TLC Rf=0.58 in 8:1 hexanes:ethyl acetate. 1H NMR (CDCl3): 7.25 (m, 1H), 6.81-6.79 (m, 3H), 6.73 (s, 1H), 5.14 (s, 1H), 4.07 (q, J=14.4, 7.2, 2H), 3.80 (s, 3H), 3.80-3.69 (m, 1H), 3.39-3.36 (m, 1H), 2.20-2.16 (m, 1H), 2.06-2.03 (m, 1H), 1.96-1.87 (m, 3H), 1.65-1.54 (m, 2H), 1.2 (t, J=1.2, 8, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093302B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-3a614e1f23b448ef9a48160ce7b521bf
출처 메모uspto-grants-2012_01