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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534166생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 4-(bromomethyl)benzoateHCID 256687—
반응물(+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehydeHCID 4692112—
용매DichloromethaneHCID 6344—
생성물Methyl 4-((3-formylpyrrolidin-1-yl)methyl)benzoateHCID 86708239—

반응 단계

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);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853408B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b2f175b161c14a34bab365342b75ed44
출처 메모uspto-grants-2014_10