Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375128Generated: October 25, 2026

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

https://huagongshe.com/reaction/2375128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
Reactant4-Fluoro-4'-methoxybenzophenoneHCID 67664—
ReactantHCID 178463197HCID 178463197—
Product1-(4-Fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-olHCID 86602779—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465415B2
Source datasetuspto-grants-2008_12
ORD IDord-ddc146cd222f4546a13cdb7193bbdee1
Source noteuspto-grants-2008_12