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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375121생성일: 2026년 10월 24일

Triphenylphosphine → N-carbobenzyloxy-4-(cis)-(4-cyanophenoxy)-L-proline methyl ester

https://huagongshe.com/ko/reaction/375121

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-CyanophenolHCID 13019—
반응물2-Methyl 1-(phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 688411—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물N-carbobenzyloxy-4-(cis)-(4-cyanophenoxy)-L-proline methyl esterHCID 1865459989%

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온도0 °C

반응 단계

To a solution of N-carbobenzyloxy-trans-4-hydroxy-L-proline methyl ester (10.0 g, 35.8 mmol) in 200 mL of anhydrous THF under N2 was added triphenylphosphine (10.6 g, 3 9.4 mmol) and 4-cyanophenol (4.7 g, 39.4 mmol) . This solution was cooled to 0° C. and then treated with diethylazodicarboxylate (6.3 mL, 39.4 mmol), added dropwise over 30 minutes The reaction was warmed to room temperature and stirred for 2 days. The solvent was removed in vacuo and the residue chromatographed (SiO2, 30% ethyl acetate/hexanes) to provide 12.1 g (89%) of N-carbobenzyloxy-4-(cis)-(4-cyanophenoxy)-L-proline methyl ester as a colorless oil. MS.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484780
출처 데이터셋uspto-grants-1996_01
ORD IDord-d581f4a9e0c24a319835f6b6689a0513
출처 메모uspto-grants-1996_01