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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519736Generated: November 4, 2026

Butyl Acetate → HCID 86679294, compound

https://huagongshe.com/reaction/1519736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl AcetateHCID 31272—
Reactant(Triisopropylsilyl)acetyleneHCID 2734682—
Reactant4-Bromo-2-furaldehydeHCID 2757010—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductHCID 86679294HCID 8667929472%

Reaction Steps

Triisopropylsilylacetylene (9.0 mL) was added dropwise to a mixture of 4-bromofuran-2-carbaldehyde (2.0 g), PdCl2(PPh3)2 (0.40 g), CuI (0.22 g), TEA (7.9 mL) and AcOBu (20 mL) at 110 to 120° C. over the course of 6 hours in a nitrogen atmosphere, and then the mixture was stirred for 2 hours. After the reaction mixture was allowed to cool, ethyl acetate (50 mL), OH type silica gel (1.0 g), cellpure (1.2 g) and activated carbon (20 mg) were added. The insolubles were filtered out, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by OH type silica gel column chromatography (gradient elution with hexane/ethyl acetate=100/0→65/35) to obtain 4-[(triisopropylsilanyl)ethynyl]furan-2-carbaldehyde (black oil) (2.3 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-b953ee4598bd4b3384e4886a5d764e2c
Source noteuspto-grants-2015_07