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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499010Generated: October 29, 2026

Water → 4-(4-Methoxy-3-methylphenyl)but-3-yn-1-ol

https://huagongshe.com/reaction/499010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-Butyn-1-OLHCID 13566—
Reactant4-Bromo-1-methoxy-2-methylbenzeneHCID 608315—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product4-(4-Methoxy-3-methylphenyl)but-3-yn-1-olHCID 6079968134.3%

Reaction Steps

A stirred solution of 4.6 grams (0.023 mole) of 5-bromo-2-methoxytoluene (commercially available), 3 mL (0.040 mole) of 3-butyn-1-ol, 0.30 gram (0.002 mole) of copper(I) iodide, 14 mL (0.100 mole) of triethylamine, and 0.25 gram (0.0004 mole) of dichlorobis(triphenylphosphine)palladium(II) in 60 mL of DMF was heated at 90° C. for about 18 hours. After this time, the reaction mixture was poured into water and extracted with diethyl ether. The ether extract was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was purified by column chromatography on silica gel using mixtures of hexane and ethyl acetate as an eluant. The appropriate fractions of eluate were combined and concentrated under reduced pressure, yielding 1.5 grams of subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767667B2
Source datasetuspto-grants-2010_08
ORD IDord-1a237645d786442fa23d078bc9c6f222
Source noteuspto-grants-2010_08