Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856022Generated: October 30, 2026

Propargyl alcohol → 3-(4-(Trifluoromethyl)phenyl)prop-2-yn-1-ol

https://huagongshe.com/reaction/856022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
CatalystTriphenylphosphineHCID 11776—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
Product3-(4-(Trifluoromethyl)phenyl)prop-2-yn-1-olHCID 1183042860%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-bromobenzotrifluoride (6.5 g, 28.89 mmol), propargyl alcohol (2.35 ml, 40.45 mmol), triethylamine (5.64 ml, 40.45 mmol), triphenylphosphine (230 mg, 0.87 mmol), cuprous iodide (110 mg, 0.58 mmol), and dichlorobis(triphenylphosphine)palladium (210 mg, 0.29 mmol) in toluene (100 ml) was stirred at 100° C. under a nitrogen atmosphere for 2 hours. The reaction mixture was allowed to return to room temperature and filtered through Celite. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate =9/1) to afford 3-(4-trifluoromethylphenyl)-2-propyn-1-ol (3.47 g, yield 60%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-cff10d4ac69946d5b443283de71be482
Source noteuspto-grants-2007_08