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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44641생성일: 2026년 10월 24일

Triphenylphosphine → N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamide

https://huagongshe.com/ko/reaction/44641

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-HydroxyacetanilideHCID 12124—
반응물4-Piperidinol, 1-methyl-HCID 66048—
용매TetrahydrofuranHCID 8028—
생성물N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamideHCID 57444159—

반응 단계

A suspension of N-(3-Hydroxy-phenyl)-acetamide (30.2 g) in anhydrous tetrahydrofuran (600 mL) was treated with 4-hydroxy-N-methylpiperidine (30.54 mL) and triphenylphosphine (68.18 g); a solution of diethylazadicarboxylate in anhydrous tetrahydrofuran (THF) (40.94 mL in 60 mL of THF) was added dropwise and the mixture was stirred at room temperature for 2 hours and then heated to 50° C. overnight. Further amounts of triphenylphosphine (28.00 g) and diethylazadicarboxylate (14 mL) were added and the heating was continued for additional 24 hours.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541429B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c4473f8be0684334b827e5bd7897e708
출처 메모uspto-grants-2013_09