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HRID 1162511作成日:2026年10月25日

Dimethylformamide → Methyl 2-(3-chloro-4-cyanophenyl)acetate

https://huagongshe.com/reaction/1162511

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 2-[3-chloro-4-(trifluoromethylsulfonyloxy)phenyl]acetateHCID 3564187—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 2-(3-chloro-4-cyanophenyl)acetateHCID 3564186—

反応条件

温度80 °C

反応手順

A solution of (3-chloro-4-trifluoromethanesulfonyloxy-phenyl)-acetic acid methyl ester 12 (24.5 g, 73.6 mmol) in dry DMF (45 mL) is combined with zinc cyanide (8.91 g, 75.9 mmol) and tetrakis(triphenylphosphine) palladium (8.50 g, 7.4 mmol). The mixture is stirred for 34 hours at 80° C., then cooled to room temperature, diluted with EtOAc (150 mL) and poured into a saturated NaHCO3 solution (150 mL). A white precipitate is removed by vacuum filtration. The organic layer of the filtrate is separated and washed with H2O. The organic layer is dried (MgSO4), filtered and concentrated. The remainder is purified by silica gel chromatography using 20% EtOAc/hexane to give (3-chloro-4-cyano-phenyl)acetic acid methyl ester 13 as a wax-like solid: 1H-NMR (400 MHz, CDCl3) δ=7.63 (d, J=8.0 Hz, 1H), 7.47 (d, J=1.2 Hz, 1H), 7.30 (dd, J=1.2 Hz, J=8.0 Hz, 1H), 3.72 (s, 3H), 3.69 (s, 2H). MS calculated for C10H9O2ClN (M+H+) 210.0, found 210.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07820705B2
出典データセットuspto-grants-2010_10
ORD IDord-1adb19982a6b4a238987ec5ea5226d8e
出典メモuspto-grants-2010_10