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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 993096생성일: 2026년 10월 26일

Bromotrimethylsilane → [2-Phenyl-1-(thiophene-2-sulfonylamino)-ethyl]phosphonic acid

https://huagongshe.com/reaction/993096

반응식

참여 물질

역할이름HCID투입량
반응물BromotrimethylsilaneHCID 76113—
반응물2-Phenyl-1-(thiophene-2-sulfonylamino)-ethyl-phosphonic Acid Diethyl EsterHCID 22890932—
용매DichloromethaneHCID 6344—
생성물[2-Phenyl-1-(thiophene-2-sulfonylamino)-ethyl]phosphonic acidHCID 2217929081.9%

반응 단계

To a solution of diethyl phosphonate (xii) (745 mg; 1.8 mmol) in dichloromethane (8 mL) at 0° C. was slowly added bromotrimethylsilane (2 mL; 15.2 mmol). The reaction was gradually warmed to room temperature and the following day the solution was evaporated. The residue was redissolved in dichloromethane (10 mL), evaporated and the process repeated once more. Methanol (10 mL) was added to the residue and the solution stirred at room temperature for 30 minutes, then the solution was filtered and concentrated. The oily residue was triturated with 1:1 ether-hexanes and the orange solid collected by filtration. Finally, the orange solid was boiled in dichloromethane (5 mL), cooled and filtered to yield pure phosphonic acid (xiii) (512 mg, 80%) as a colorless solid: 1H NMR (400 MHz, CD3OD) δH 2.71 (dt, J=14, 10 Hz, 1H, CHPh), 3.13 (ddd, J=4, 8, 14 Hz, 1H, CHPh), 3.89 (ddd, J=4, 10, 14 Hz, NCHP), 6.86 (dd, J=3.5, 5 Hz, 1H, Ar—H), 7.07-7.15 (m, 6H, Ar—H), 7.53 (dd, J=1.5, 5 Hz, 1H, Ar—H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06472406B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-3ee8195dd3bf4596a98e1b62d739dcd4
출처 메모uspto-grants-2002_10