돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557776생성일: 2026년 10월 24일

p-Fluoronitrobenzene → Methyl 1-(4-nitrophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/557776

반응식

참여 물질

역할이름HCID투입량
반응물p-FluoronitrobenzeneHCID 9590—
반응물DiisopropylethylamineHCID 81531—
반응물Methyl isonipecotateHCID 424914—
용매TetrahydrofuranHCID 8028—
생성물Methyl 1-(4-nitrophenyl)piperidine-4-carboxylateHCID 34500237.4%

반응 조건

온도150 °C

반응 단계

To a solution of 4-fluoronitrobenzene (0.70 g, 4.96 mmol) in THF (8 mL) was added piperadine-4-carboxylic acid methyl ester (0.71 g, 4.96 mmol) and diisopropylethylamine (0.66 g, 5.11 mmol). The mixture was heated in a microwave oven at 150° C. for 1.5 hr. The resulting mixture was extracted with ethyl acetate and hydrochloric acid (0.2 N). The organic layer was washed with brine and concentrated sodium bicarbonate solution. After the evaporation of solvents, the residue was purified through a Biotage flash column chromatography using ethyl acetate and hexanes (1:1 ratio) to give a yellow solid as 1-(4-nitrophenyl)-piperidine-4-carboxylic acid methyl ester (490 mg). 1H-NMR is consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058299B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-a53dc576db814d0182597ed153ed5dee
출처 메모uspto-grants-2011_11