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HRID 418891作成日:2026年10月26日

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

https://huagongshe.com/reaction/418891

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
反応物2-(3-Methoxyphenyl)cyclohexanoneHCID 85868—
溶媒TolueneHCID 1140—
生成物Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetateHCID 5372010899.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093302B2
出典データセットuspto-grants-2012_01
ORD IDord-3a614e1f23b448ef9a48160ce7b521bf
出典メモuspto-grants-2012_01