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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061591Generated: November 2, 2026

Propargyl alcohol → HCID 11672832, compound

https://huagongshe.com/reaction/1061591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant3,4-DibromothiopheneHCID 18452—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventPropylamineHCID 7852—
ProductHCID 11672832HCID 1167283287.4%

Reaction Steps

Pd(Ph3P)4 (116 mg, 2%), CuI (28 mg, 3%) and propargyl alcohol (0.9 ml, 15 mmol) are added successively to a solution of 3,4-dibromothiophene (1.18 g, 5.0 mmol) in n-propylamine (15 ml), and the reaction mixture is stirred at RT for 1 h and then under reflux for 7 h. More Pd(Ph3P)4 (58 mg, 1%), CuI (14 mg, 1.5%) and propargyl alcohol (0.45 ml, 7.5 mmol) are then added and the mixture is stirred under reflux for another 8 h. After cooling, the reaction mixture is filtered off through kieselguhr and washed with ethyl acetate (20 ml). The organic phase is concentrated under reduced pressure. Further purification is carried out by chromatography [Tol/Ac (8:2)] over a silica gel column. This gives the title compound (0.84 g) as a colorless solid. TLC, silica gel (glass plates), [toluene/acetone (8:2)], Rf=0.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960588B1
Source datasetuspto-grants-2005_11
ORD IDord-600e136ea1304ba4969fa00fb432e449
Source noteuspto-grants-2005_11