돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345071생성일: 2026년 10월 25일

Triphenylphosphine → 9-[1-(t-Butyldimethylsilyloxy)-4-(diethoxyphosphorylmethoxy)but-2-oxy]-6-phthalimidopurine

https://huagongshe.com/reaction/345071

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물9-Hydroxy-6-phthalimidopurineHCID 14523970—
반응물HCID 19993524HCID 19993524—
용매TetrahydrofuranHCID 8028—
생성물9-[1-(t-Butyldimethylsilyloxy)-4-(diethoxyphosphorylmethoxy)but-2-oxy]-6-phthalimidopurineHCID 1999354569.3%

반응 조건

온도20 °C

반응 단계

A solution of diethyl 4-t-butyldimethylsilyloxy-3-hydroxybutoxymethylphosphonate (0.49 g, 1.31 mmol), 9-hydroxy-6-phthalimidopurine (0.5 g, 1.31 mmol) and triphenylphosphine (0.52 g, l.97 mmol) in dry tetrahydrofuran (50 ml) was stirred under nitrogen at O° C. during the addition of diethyl azodicarboxylate (0.31 ml, 1.97 mmol). The solution was then stirred at 20° C. for 4 h and evaporated in vacuo. The residue was chromatographed on silica, eluting with hexane-acetone 4:1, affording 9-[1-(t-butyldimethylsilyloxy)-4-(diethoxyphosphorylmethoxy)but-2-oxy]-6-phthalimidopurine (575mg, 69%) as a clear oil. νmax (film) 3500, 1790, 1740, 1600 and 1580 cm-1 ; δH [(CD3)2SO] 0.04 (6H, s, CH3SiCH3), 0.74 (9H, s, (CH3)3CSi), 1.22 (6H, t, J6.9 Hz, 2×CH3CH 2), 2.04 (2H, m, SiOCH2CHCH2), 3.79 (2H, m, CH2OSi), 3.88 (2H, d, J8.2 Hz, CH2P), 3.96 (2H, m, CH2OCH2P), 4.03 (4H, m, 2×CH3CH2), 4.69 (1H, m, CHON), 8.05 (4H, m, ArH), 8.91 (1H, s, H-2/H-8), 9.07 (1H, s, H-2/H-8); m/z (FAB+ve Ion), 656 (MNa+) and 634 (MH+). Found: C, 53.10 H, 6.30; N, 10.83%; C28H40N5O8PSi requires C, 53.07; H, 6.36,; N, 11.05%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05055458
출처 데이터셋uspto-grants-1991_10
ORD IDord-d0b43dfccfdf4ca88bd8794b186fd02f
출처 메모uspto-grants-1991_10