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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552277생성일: 2026년 10월 26일

5-Ethyl-4-phenyl-thiophene-2-carboxylic acid → 1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanone

https://huagongshe.com/reaction/552277

반응식

참여 물질

역할이름HCID투입량
반응물5-Ethyl-4-phenyl-thiophene-2-carboxylic acidHCID 67166421—
반응물HCID 178418348HCID 178418348—
용매TetrahydrofuranHCID 8028—
생성물1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanoneHCID 67166164—

반응 단계

At 5° C. a solution of 5-ethyl-4-phenyl-thiophene-2-carboxylic acid (180 mg, 0.775 mmol) in THF (4 mL) is treated with MeLi (0.9 mL, 1.6 M in diethyl ether). The reaction mixture is stirred at rt for 30 min before another portion of MeLi (0.5 mL) is added. Stirring is continued for 1 h, the reaction is quenched by adding water (50 mL) and extracted with EA. The organic extract is dried over MgSO4, the solvent is removed in vacuo, and the crude product is purified by CC on silica gel eluting with heptane:EA 30:1 to give 1-(5-ethyl-4-phenyl-thiophen-2-yl)-ethanone (64 mg) as a colourless oil; LC-MS: tR=1.03 min, [M+1+MeCN]+=272.15; 1H NMR (CDCl3): δ 7.60 (s, 1H), 7.47-7.32 (m, 5H), 2.91 (q, J=7.6 Hz, 2H), 2.54 (s, 3H), 1.30 (t, J=7.6 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951794B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-105c59f248dc4ed9bae4ef820754fe68
출처 메모uspto-grants-2011_05