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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414583생성일: 2026년 10월 24일

Sodium hydride → 2-(4-Chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)ethene

https://huagongshe.com/ko/reaction/414583

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Diethyl 4-chlorobenzylphosphonateHCID 99240—
반응물5-(5-Methylthiophen-2-yl)thiophene-2-carbaldehydeHCID 4987278—
용매DimethylformamideHCID 6228—
생성물2-(4-Chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)etheneHCID 54303521—

반응 단계

Under a nitrogen atmosphere, 0.12 gram (0.0050 mole) of sodium hydride was added to a stirred solution of 1.2 gram (0.0057 mole) of 5-formyl-5'-methyl[2,2'-bithienyl] and 1.7 gram (0.0064 mole) of diethyl 4-chlorobenzylposphonate in 20 mL of N,N-dimethylformamide. The reaction mixture was stirred at room temperature for about three huurs. Analysis of the reaction mixture by thin layer chromatography indicated starting materials remained. Additional sodium hydride was added, and the mixture was stirred at room temperature for several hours. The reaction mixture was quenched with an aqueous solution saturated with ammonium chloride. This mixture was extracted several times with diethyl ether. The extracts were combined and washed with an aqueous solution saturated with sodium chloride. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving a residue. This residue was purified by column chromatography on silica gel to yield 2-(4-chlorophenyl)-1-(5'-methyl[2,2'-bithienyl]-5-yl)ethene as a solid, m.p. 157°-162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04792567
출처 데이터셋uspto-grants-1988_12
ORD IDord-dd85b256c9904ba0912b9d199ba67bd7
출처 메모uspto-grants-1988_12