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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 660477생성일: 2026년 10월 24일

Isocyanate → 5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one

https://huagongshe.com/ko/reaction/660477

반응식

참여 물질

역할이름HCID투입량
반응물IsocyanateHCID 105034—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756937—
용매TetrahydrofuranHCID 8028—
생성물5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-oneHCID 68838643—

반응 단계

Tetrabutylammonium fluoride (1.0M in THF, 15 mL) is added to a solution of PS-isocyanate resin (3.5 g) in THF. The mixture is stirred at RT for 2 h. The resin is filtered off and the filtrate is added to a solution of 5-(2-benzyloxy-4-iodophenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (5.0 g, 9.18 mmol) in THF. The reaction is stirred at 50° C. for 18 h. The mixture is cooled and concentrated. The residue is partitioned between EtOAc and water and the organic layer is washed with 1N HCl (5×50 mL) and brine. The organic layer is dried over Na2SO4 and concentrated. The residue is purified by reverse phase chromatography using a 10-60% gradient of EtOH/water as eluent to afford the title compound as a light yellow solid: (M−1)−=442.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084448B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-a83f45cde89f4f848cb5f96f5240b938
출처 메모uspto-grants-2011_12