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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225393생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/225393

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 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 NH4Cl (200 mL), saturated aqueous NaCl (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 번호US07556751B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-ba0ce24846e3467bbeefbf4f3f25d544
출처 메모uspto-grants-2009_07