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HRID 534166作成日:2026年10月24日

Trifluoroacetic acid → Methyl 4-((3-formylpyrrolidin-1-yl)methyl)benzoate

https://huagongshe.com/ja/reaction/534166

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 4-(bromomethyl)benzoateHCID 256687—
反応物(+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehydeHCID 4692112—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-((3-formylpyrrolidin-1-yl)methyl)benzoateHCID 86708239—

反応手順

Tert-Butyl 3-formylpyrrolidine-1-carboxylate (4.75 g, 23.84 mmol) was dissolved in dichloromethane (DCM) (20 mL). Trifluoroacetic acid (15 mL, 195 mmol) was added and the reaction mixture was stirred at room temperature for 1 hour. After concentrating acetonitrile (100 mL) was added followed by methyl 4-(bromomethyl)benzoate (6.55 g, 28.6 mmol) and potassium carbonate (16.47 g, 119 mmol). The reaction was heated to reflux for 16 hours. The mixture was filtered and concentrated. Dichloromethane (75 ml) was added and the solution was washed with water, dried over MgSO4, filtered and concentrated. The residue was purified via silica gel chromotography (0% to 100% EtOAc:Hex; 50 g-HP-silica gel column). Obtained 2.00 g 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.99-2.23 (m, 2H), 2.46-2.57 (m, 1H), 2.60-2.79 (m, 2H), 2.88-2.99 (m, 2H), 3.68 (d, J=4.29 Hz, 2H), 3.92 (s, 3H), 7.40 (d, J=8.59 Hz, 2H), 7.93-8.09 (m, 2H), 9.66 (d, J=2.02 Hz, 1H);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853408B2
出典データセットuspto-grants-2014_10
ORD IDord-b2f175b161c14a34bab365342b75ed44
出典メモuspto-grants-2014_10