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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429281Generated: October 31, 2026

Hydrochloric Acid → HCID 68109356, compound

https://huagongshe.com/reaction/1429281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropargyl alcoholHCID 7859—
ReactantDiisopropylamineHCID 7912—
Reactant6-Bromo-2-naphthalenolHCID 27144—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68109356HCID 68109356—

Reaction Steps

9.00 g (40.3 mmol) of 6-bromonaphthalen-2-ol, 3.5 g (62.4 mmol) of prop-2-yn-1-ol, 1.00 g (1.43 mmol) of bis(triphenylphosphine)palladium(II) chloride, 0.5 g (2.63 mmol) of copper(I) iodide and 10 ml of diisopropylamine are left to stir overnight at 80° C. in 60 ml of DMF. The batch is subsequently added to 200 ml of ethyl acetate, 400 ml of water are added, and the mixture is acidified using hydrochloric acid. The aqueous phase is separated off and extracted three times with ethyl acetate. The combined org. phases are evaporated in vacuo, and the residue is filtered through silica gel with toluene/ethyl acetate (2:1). Crystallisation of the crude product from toluene/heptane gives 6-(3-hydroxyprop-1-ynyl)naphthalen-2-ol as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940184B2
Source datasetuspto-grants-2015_01
ORD IDord-42e236eea22c4664b6c01be09988e97e
Source noteuspto-grants-2015_01