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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291597Generated: October 30, 2026

Propargyl alcohol → 5-(3-Hydroxy-1-propynyl)-2,2'-bithiophene

https://huagongshe.com/reaction/1291597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Iodo-2,2'-bithiopheneHCID 11323778—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystBenzyl triethylammonium chlorideHCID 66133—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
Product5-(3-Hydroxy-1-propynyl)-2,2'-bithiopheneHCID 1892044174%

Reaction Steps

To the mixture of 48 mg (0.86 mmole) of propargyl alcohol, 1 ml of benzene, 0.1 g of 5-iodo-2,2'-bithiophene (0.34 mmole) was added 0.25 g of CuI, 0.05 g of benzyltriethylammonium chloride and 0.1 g of Pd(PPh3)4. To the solution, 3 ml of NaOH solution (2.5 N) was added at room temperature and stirred for 2 hours. 4 ml of NH4Cl solution was then added. The reaction solution was extracted with 50 ml of ethyl acetate. The extract was washed with 10 ml of HCl (10%) for 3 times, 50 ml of water twice and dried over anhydrous magnesium sulfate. The residual solid was purified by silica gel column chromatography. From the eluate of ethyl acetate/n-hexane (3/1) 56 mg of product (74%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753692
Source datasetuspto-grants-1998_05
ORD IDord-6d87f343c025411bb1f67f975173002c
Source noteuspto-grants-1998_05