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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873396생성일: 2026년 10월 27일

N-Formylmorpholine → 5-(4-Ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehyde

https://huagongshe.com/reaction/1873396

반응식

참여 물질

역할이름HCID투입량
반응물N-FormylmorpholineHCID 20417—
반응물2-(4-Ethoxy-2,3-difluorophenyl)selenopheneHCID 59456301—
반응물ButyllithiumHCID 178418339—
용매Hydrochloric AcidHCID 313—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물5-(4-Ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehydeHCID 59456315—

반응 단계

7.6 ml (44.4 mmol) of TMP are initially introduced at −20° C. in THF, and 26.7 ml (42.4 mmol, 15% soln. in hexane) of n-BuLi are metered in. After 25 min at this temperature, a solution of 11.7 g (38.6 mmol) of 2-(4-ethoxy-2,3-difluorophenyl)selenophene in 80 ml of THF is added. When the addition is complete, the batch is warmed to RT over the course of 45 min and left at this temperature for 20 min. The solution is cooled to −40° C., and N-formylmorpholine is added. The reaction mixture is warmed to RT and stirred for 4.5 h. The solution is diluted with a lot of dichloromethane, and 2 N hydrochloric acid is added. The mixture is briefly stirred vigorously, and the organic phase is separated off. The aqueous phase is extracted with dichloromethane, and the combined organic phases are washed with water. The solution is dried using sodium sulfate and concentrated to dryness. The residue is digested in cold ethanol, and the solid is filtered off with suction. Drying in vacuo gives 5-(4-ethoxy-2,3-difluorophenyl)selenophene-2-carbaldehyde as a violet solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304036B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-88a5c4f7866d4e3bb8f717dfa949ce84
출처 메모uspto-grants-2012_11