Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330821Generated: October 24, 2026

Tributylamine → HCID 66691768, compound

https://huagongshe.com/en/reaction/330821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantEthyl AcetateHCID 8857—
Reactant3,3-Diethoxy-1-propeneHCID 62477—
ReactantHCID 66691575HCID 66691575—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 66691768HCID 66691768—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 1.80 g (5.17 mmol) 1-ethoxy-4-((4-iodophenyl)ethynyl)benzene (XII.1) in 24 mL DMF are added 2.36 mL (15.5 mmol) 3,3-diethoxy-propene, 3.69 mL (15.5 mmol) tributylamine, 1.44 g (5.17 mmol) tetrabutylammoniumchloride and 0.04 g (0.16 mmol) palladium(II)acetate under argon. The mixture is stirred at 120° C. for 12 h. After that time, 1.18 mL (7.76 mmol) 3,3-diethoxy-propene are added and the mixture is stirred at 120° C. for 5 d. After cooling, EtOAc is added and the mixture is washed with 1N potassium hydrogensulfate solution and water. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; PE:DCM 1:1) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877754B2
Source datasetuspto-grants-2014_11
ORD IDord-caeaae0a8b5941e9b57e00af235f045f
Source noteuspto-grants-2014_11