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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 463340생성일: 2026년 10월 24일

Triphenylphosphine → Ethyl [5-{5-(4-methoxy-3-propylphenyl)pentyloxy}-1-naphthalenyloxy]acetate

https://huagongshe.com/ko/reaction/463340

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물5-(4-Methoxy-3-propylphenyl)pentanolHCID 20282931—
반응물Ethyl(5-hydroxy-1-naphthalenyloxy)acetateHCID 20475151—
용매TetrahydrofuranHCID 8028—
생성물Ethyl [5-{5-(4-methoxy-3-propylphenyl)pentyloxy}-1-naphthalenyloxy]acetateHCID 5457478279.5%

반응 단계

To a stirred suspension of 5-(4-methoxy-3-propylphenyl)pentanol (2.48 g), ethyl (5-hydroxy-1-naphthalenyloxy)acetate (2 g), and triphenylphosphine (3.2 g) in dry tetrahydrofuran (30 ml) under nitrogen was added diethyl azodicarboxylate (1.65 ml) slowly so that the temperature did not rise above 50°. After 3 hours the solution was evaporated, and the residue was chromatographed on silica with a mixture of dichloromethane and light petroleum (bp 40°-60°) (4:6) to give the sub-title ester (3 g), mp 70° (from ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04518612
출처 데이터셋uspto-grants-1985_05
ORD IDord-ebc4e97402b44fd087f7b97509c1aa7e
출처 메모uspto-grants-1985_05