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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511060Generated: November 2, 2026

Hydrochloric Acid → HCID 66798230, compound

https://huagongshe.com/reaction/511060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
Reactant3-Butyn-1-OLHCID 13566—
ReactantHCID 66798094HCID 66798094—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66798230HCID 66798230—

Reaction Steps

9.0 g (24.6 mmol) of 7-iodo-9,10-dihydrophenanthren-2-ol are initially introduced in 100 ml of THF, 1.0 g (1.43 mmol) of bis(triphenylphosphine)palladium(II) chloride, 0.3 g (1.58 mmol) of copper(I) iodide and 11 ml of diisopropylamine are added, and subsequently a solution of 3.0 g (42.8 mmol) of but-3-yn-1-ol in 20 ml of THF is added dropwise at max. 30° C. with gentle cooling. The batch is left to stir at room temp. for 1.5 h, added to water and acidified using 2 N hydrochloric acid. The aqueous phase is separated off and extracted three times with ethyl acetate. The combined org. phases are washed with water, dried over sodium sulfate, and the solvent is removed in vacuo. The crude product is filtered through silica gel with dichloromethane/ethyl acetate (3:1) and recrystallised from toluene, giving 7-(4-hydroxybut-1-ynyl)-9,10-dihydrophenanthren-2-ol as colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096795B2
Source datasetuspto-grants-2015_08
ORD IDord-57be430b8a664c8d92af4503c09059a0
Source noteuspto-grants-2015_08