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HRID 333279作成日:2026年10月26日

Methyl Acrylate → Dimethyl 3-cyano-3-(naphthalen-2-yl)hexanedioate

https://huagongshe.com/reaction/333279

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl AcrylateHCID 7294—
反応物2-NaphthylacetonitrileHCID 82008—
溶媒tert-ButanolHCID 6386—
溶媒Methanol tert-butyl alcoholHCID 19609033—
生成物Dimethyl 3-cyano-3-(naphthalen-2-yl)hexanedioateHCID 6867300985.8%

反応手順

2-naphthylacetonitrile (3.45 g, 20.6 mmol) and methyl acrylate (9.7 ml, 107 mmol) were suspended in 2-methyl-2-propanol (10 ml). Heat was applied to the reaction vessel until the solution became clear. The mixture was cooled to room temperature, at which time (Bu)4NOH (6.9 mmol, 0.33 equiv.) was added as a solution in 2-methyl-2-propanol:methanol (1:2). The combined reaction mixture was heated to reflux for 4 h under vigorous stirring at which time the reaction appeared complete by GC-MS. After allowing the reaction to cool the mixture was partitioned between H2O (75 ml) and EtOAc (50 ml). The aqueous layer was removed and washed with EtOAc (2×50 ml). The combined organic phases were washed with NaHCO3 (sat. aq.) and brine and dried over MgSO4. After filtration the solvent was removed in vacuo. The crude product was purified by flash column chromatography (25% EtOAc in hexanes) to isolate the title compound as a light yellow oil (5.75 g, 82%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877975B2
出典データセットuspto-grants-2014_11
ORD IDord-f1b69c4742fd484d851d820cc28162d0
出典メモuspto-grants-2014_11