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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419313생성일: 2026년 10월 23일

Triphenylphosphine → HCID 59452627, 화합물

https://huagongshe.com/ko/reaction/419313

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Methyl-4-nitrophenolHCID 17412—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Benzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
용매DichloromethaneHCID 6344—
생성물HCID 59452627HCID 5945262787%

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온도0 °C

반응 단계

3-Methyl-4-nitrophenol (1.74 g, 11.4 mmol), triphenylphosphine (5.98 g, 22.8 mmol), and phenylmethyl 4-hydroxy-1-piperidinecarboxylate (3.99 g, 17.0 mmol) were dissolved in DCM with stirring and cooled to 0° C. Diisopropyl azodicarboxylate (3.35 mL, 17.0 mmol) was added via syringe. The reaction was stirred for 10 min and allowed to warm to rt. The reaction was stirred overnight and adsorbed onto silica gel. The crude material was purified by flash chromatography, and fractions containing product were concentrated in vacuo. The material was contaminated with 3-methyl-4-nitrophenol. The material was dissolved in diethyl ether and washed with 2N NaOH solution (3×), H2O, and brine. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to provide 3.67 g (87%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ 8.02 (d, J=9.0 Hz, 1H), 7.42-7.24 (m, 5H), 7.06 (d, J=2.4 Hz, 1H), 7.01 (dd, J=9.1, 2.7 Hz, 1H), 5.07 (s, 2H), 4.76 (ddd, J=7.7, 4.2, 4.0 Hz, 1H), 3.81-3.64 (m, 2H), 3.31 (br. s., 2H), 2.52 (s, 3H), 2.01-1.88 (m, 2H), 1.63-1.49 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093239B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-d6bad6fa66c74a7881dd631728f4e66b
출처 메모uspto-grants-2012_01