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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429283Generated: November 1, 2026

Hydrochloric Acid → HCID 66798230, compound

https://huagongshe.com/reaction/1429283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-ButyneHCID 7846—
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 66798094HCID 66798094—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
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 a solution of 3.0 g (42.8 mmol) of 1-butyne in 20 ml of THF is subsequently added dropwise with cooling at max. 30° C. 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 a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940184B2
Source datasetuspto-grants-2015_01
ORD IDord-35b34baf4df5450897b498c9d526986c
Source noteuspto-grants-2015_01