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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241995생성일: 2026년 10월 24일

Triethylamine → Ethyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoate

https://huagongshe.com/ko/reaction/241995

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 296342—
반응물4-Acetamidobenzenesulfonyl azideHCID 5129185—
용매AcetonitrileHCID 6342—
생성물Ethyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoateHCID 76818128—

반응 조건

온도0 °C

반응 단계

Ethyl 3-(2-fluorophenyl)-3-oxopropanoate (1.00 g, 4.76 mmol) was dissolved in acetonitrile (14 mL) and treated with triethylamine (0.760 ml, 5.47 mmol, 1.15 equiv). The mixture was cooled to 0° C., treated with 4-acetamidobenzenesulfonylazide (1.26 g, 5.23 mmol, 1.1 equiv) and warmed to ambient temperature over 1.5 hours. The mixture was partially concentrated in vacuo, cooled to 0° C., treated with sodium hydroxide (50 mL, 1 N aqueous) and extracted with chloroform (3×50 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel gradient chromatography (100:0 to 85:15; hexanes:ethyl acetate) providing the titled compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653079B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-6ab024c191ed49abb57df564e3e0ab5e
출처 메모uspto-grants-2014_02