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HRID 715997作成日:2026年10月26日

(Triphenylphosphoranylidene)acetonitrile → (E)-Methyl 4,5-dichloro-2-(2-cyanovinyl)benzoate

https://huagongshe.com/reaction/715997

反応式

関与物質

役割名称HCID仕込み量
反応物(Triphenylphosphoranylidene)acetonitrileHCID 85524—
反応物Methyl 4,5-dichloro-2-formylbenzoateHCID 86647797—
溶媒TolueneHCID 1140—
生成物(E)-Methyl 4,5-dichloro-2-(2-cyanovinyl)benzoateHCID 86647796—

反応手順

A mixture of the product from Example 56C (2.0 g, 8.6 mmol) and (triphenylphosphoranylidene)acetonitrile (2.87 g, 9.5 mmol) in toluene (30 mL) was refluxed for 24 hours. The reaction was cooled to room temperature and filtered through a short plug of silica gel eluting with diethyl ether to remove the triphenyl phosphine oxide. The filtrate was concentrated and the residue was purified via flash chromatography on a silica gel:column (5:95 ethyl acetate:hexane) to afford the title compound and the corresponding Z isomer. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.88 (s, 3H) 6.55 (d, J=16.27 Hz, 1H) 8.05 (d, J=16.95 Hz, 1H) 8.09 (s, 1H) 8.13 (s, 1H); MS (DCI+) m/z 273.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187483B2
出典データセットuspto-grants-2015_11
ORD IDord-13a5e6b49ab040bd9fbfb79bae8bcdbe
出典メモuspto-grants-2015_11