Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901766Generated: November 2, 2026

Sodium Hydroxide → 5-(3-Hydroxy-1-propynyl)-2,2'-bithiophene

https://huagongshe.com/reaction/1901766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantProp-1-yn-1-olHCID 6432594—
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 1892044174.3%

Reaction Steps

Hydroxy-1-propyne (48 mg) was dissolved in benzene (1 ml). 5-Iodo-2,2'-bithiophene (0.1 g) was added immediately and stirred. A mixture of CuI (0.05 g), benzyltriethylammonium chloride (0.05 g), catalyst Pd(PPh3)4 (0.1 g) and 3 ml of NaOH solution (2.5N) were mixed together at room temperature and stirred for 2 hours. NH4Cl solution (4 ml) was then added. The reaction solution was extracted with 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, eluted with ethyl acetate/n-hexane (3/1) to yield 56 mg of the product (74% ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578636
Source datasetuspto-grants-1996_11
ORD IDord-8894311ad013430c888ea0e172e2dce2
Source noteuspto-grants-1996_11