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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 906347생성일: 2026년 10월 24일

3-Fluorophenol → Tert-butyl 4-(3-fluorophenoxy)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/906347

반응식

참여 물질

역할이름HCID투입량
반응물3-FluorophenolHCID 9743—
반응물TriphenylphosphineHCID 11776—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(3-fluorophenoxy)piperidine-1-carboxylateHCID 5769952094.1%

반응 단계

To a solution of 1,1-dimethylethyl 4-hydroxy-1-piperidinecarboxylate (24 g, 112 mmol), 3-fluorophenol (5.6 g, 59 mmol) and triphenylphosphine (31.4 g, 118 mmol) in THF (100 ml) was added di-isopropylazodicarboxylate (23.3 ml, 118 mmol). The reaction was stirred at room temperature over-weekend and then the solvent was removed in vacuo. The residue was diluted with DCM, hexane was added and the resultant precipitate was filtered off. The filtrate was concentrated in vacuo and purified by column chromatography. Elution with DCM gave the title compound (16.4 g, 87% pure). δH (CDCl3, 250 MHz) 1.47 (9H, s), 1.76 (2H, m), 1.92 (2H, m), 3.35 (2H, ddd), 3.69 (2H, ddd), 4.44 (1H, m), 6.65 (3H, m), 7.20 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012981B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-653c2f53d16b4ac2a8f39fa0090f1622
출처 메모uspto-grants-2011_09