돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724617생성일: 2026년 10월 26일

Triphenylphosphine → 2-{3-[3-(2-Tert-butyl-1,1,3-trioxo-2,3-dihydro-1h-1lambda6-isothiazol-5-yl)-phenyl]-propoxy}-6-hydroxy-benzoic acid methyl ester

https://huagongshe.com/reaction/724617

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Methyl 2,6-dihydroxybenzoateHCID 519869—
반응물HCID 58746837HCID 58746837—
용매TetrahydrofuranHCID 8028—
생성물2-{3-[3-(2-Tert-butyl-1,1,3-trioxo-2,3-dihydro-1h-1lambda6-isothiazol-5-yl)-phenyl]-propoxy}-6-hydroxy-benzoic acid methyl esterHCID 69598041—

반응 조건

온도25 °C

반응 단계

A solution of 4.08-C (0.21 g, 0.6 mmol), methyl 2,6-dihydroxybenzoate (0.13 g, 0.8 mmol), and triphenylphosphine (0.22 g, 0.8 mmol) in tetrahydrofuran (1.5 mL) was treated with diisopropyl azodicarboxylate (0.18 mL, 0.9 mmol) dropwise at 0° C. The reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated to give a crude residue which was purified using flash column chromatography (100% hexane to 25% ethyl acetate/hexane) to yield 4.08-D as a white solid (0.18 g, 60%). 1H NMR (500 MHz, CDCl3): δ 11.47 (s, 1H), 7.42 (dd, J=8.3, 8.3 Hz, 1H), 7.34–7.31 (m, 3H), 7.11–7.08 (m, 1H), 6.62 (s, 1H), 6.60 (dd, J=8.3, 1.0 Hz, 1H), 6.43 (dd, J=8.3, 1.0 Hz, 1H), 4.27–4.25 (m, 2H), 4.21–4.19 (m, 2H), 3.91 (s, 3H), 2.33–2.30 (m, 2H), 1.73 (s, 9H); LCMS found for C24H27NO8SNa (M+Na)+: m/z=512.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141596B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-4e37e175629544f8a22e747b43485298
출처 메모uspto-grants-2006_11