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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2375128생성일: 2026년 10월 26일

Acetylene → 1-(4-Fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-ol

https://huagongshe.com/reaction/2375128

반응식

참여 물질

역할이름HCID투입량
반응물AcetyleneHCID 6326—
반응물4-Fluoro-4'-methoxybenzophenoneHCID 67664—
반응물HCID 178463197HCID 178463197—
생성물1-(4-Fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-olHCID 86602779—

반응 단계

4-fluoro-4′-methoxy-benzophenone from Step 1 (126.7 grams) and acetylene saturated N,N-dimethylformamide (380 mL) were combined in a reaction flask. Sodium acetylide solution (9% by weight in toluene, 343 grams) was added to the reaction mixture dropwise over 45 minutes. The reaction mixture was stirred at room temperature for 1 hour and then poured into ice water (600 mL). The layers were phase separated and the aqueous layer was extracted with three portions of diethyl ether (200 mL). The organic layers were combined and washed with saturated aqueous ammonium chloride (200 mL), saturated aqueous sodium chloride (200 mL), and saturated aqueous sodium bicarbonate (200 mL). The organic layer was dried over anhydrous sodium sulfate and evaporated to an amber colored oil yielding 136.6 grams of 1-(4-fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-ol. This material was not purified further but was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07465415B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-ddc146cd222f4546a13cdb7193bbdee1
출처 메모uspto-grants-2008_12