돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481377생성일: 2026년 10월 25일

Triethylamine → 3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-one

https://huagongshe.com/reaction/481377

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(Phenylthio)acetic acidHCID 59541—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Bromo-4'-(methylsulfonyl)acetophenoneHCID 735823—
용매AcetonitrileHCID 6342—
생성물3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-oneHCID 10269135—

반응 조건

온도0 °C

반응 단계

At 0° C., triethylamine (335 μL) was added to a solution of thiophenoxyacetic acid (161 mg) and 2-bromo-l-(4-(methylsulfonyl) phenyl) ethanone (272 mg, WO 9500501, example 9, Step 1) in 5 mL of acetonitrile and the mixture was stirred at 0° C. for 1 h. The reaction mixture was then cooled to -20° C. and DBU (265 μL) was added. The mixture was stirred for 30 min. at -20° C. and was quenched by addition of 1N HCl. The product was extracted with EtOAc, dried over sodium sulfate and partially purified by silica gel chromatography. The impure product was recrystalized from EtOAc/Hexane to afford the title compound as a solid

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789413
출처 데이터셋uspto-grants-1998_08
ORD IDord-6197c4ee24984d6da99e2e74b559676a
출처 메모uspto-grants-1998_08