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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651516생성일: 2026년 10월 26일

Triphenylphosphine → 3-Chlorobenzenesulfonic Acid 3-[[N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]-5-methylphenyl Ester

https://huagongshe.com/reaction/651516

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
반응물3-(3-Chlorophenylsulfonyloxy)-5-methylphenolHCID 54017679—
용매TetrahydrofuranHCID 8028—
생성물3-Chlorobenzenesulfonic Acid 3-[[N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]-5-methylphenyl EsterHCID 5424433681%

반응 조건

온도0 °C

반응 단계

Diethyl azodicarboxylate (349 mg, 2.0 mmol) was added to a solution of 3-chlorobenzenesulfonic acid 3-hydroxy-5-methylphenyl ester (600 mg, 2.0 mmol), as prepared in the preceding step, N-tert-butoxycarbonyl-4-piperidinemethanol (430 mg, 2.0 mmol), as prepared in step (b) of Example 1, and triphenylphosphine (525 mg,. 2.0 mmol) in tetrahydrofuran (20 mL) at 0° C. The mixture was stirred at 0° C. for 2 H and at room temperature for 3 H. The reaction was quenched with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic phase was washed with saturated NaHCO3 (2×50 mL), brine (2×50 mL) and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (1:3 ethyl acetate/hexane) to give the tide compound as a colorless liquid (800 mg, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06281206B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-badd37c29c8946bcbae7f4830ea64a72
출처 메모uspto-grants-2001_08