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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23533생성일: 2026년 10월 23일

Triphenylphosphine → [4-(Tetrahydro-pyran-4-yloxy)-naphthalen-1-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/23533

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Tetrahydro-4H-pyran-4-olHCID 74956—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물tert-Butyl (4-hydroxynaphthalen-1-yl)carbamateHCID 10923237—
용매TetrahydrofuranHCID 8028—
생성물[4-(Tetrahydro-pyran-4-yloxy)-naphthalen-1-yl]-carbamic acid tert-butyl esterHCID 2075658055%

반응 조건

온도0 °C

반응 단계

Triphenylphosphine (2.8 g, 10.8 mmol) was dissolved in THF (5 mL) and cooled to 0° C. To this colorless solution diethylazodicarboxylate (1.9 grams, 10.8 mmol) was added dropwise to afford an orange solution. After 15 min at 0° C., a copious precipitate had formed. 4-Hydroxy-naphthalen-1-yl-carbamic acid tert-butyl ester (934 mg, 3.6 mmol) and tetrahydro-4H-pyran-4-ol (552 mg, 5.4 mmol) were then added in one portion as a solution in 2 mL of THF. The purple suspension was stirred at 0° C. for one h then at room temperature for 48 h. The solvent was then evaporated and chromatographed on silica gel (40% EtOAc-hexanes) to provide 680 mg (55%) of [4-(tetrahydro-pyran-4-yloxy)-naphthalen-1-yl]-carbamic acid tert-butyl ester as a purple solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852717B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-3ce72494a05e4cd89083727714415d7a
출처 메모uspto-grants-2005_02