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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078231Generated: November 1, 2026

3,3,3-Triethoxyprop-1-yne → Ethyl 3-(2-bromo-5-chlorophenyl)propiolate

https://huagongshe.com/reaction/2078231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,3-Triethoxyprop-1-yneHCID 10920972—
Reactant1-Bromo-4-chloro-2-iodobenzeneHCID 51000072—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(2-bromo-5-chlorophenyl)propiolateHCID 6709933855.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

A suspension of 1-bromo-4-chloro-2-iodobenzene (5.4 g, 17.0 mmol), 3,3,3-triethoxyprop-1-yne (4.4 g, 25.6 mmol), copper(I) iodide (976 mg, 5.1 mmol), and trans-dichlorobis(triphenylphosphine)palladium(II) (1.19 g, 1.7 mmol) in ACN (60 mL) was degassed and backfilled with argon. The resulting mixture was treated with TEA (22.0 mL, 157.9 mmol). The reaction flask was capped with a septum and stirred at 23° C. After 90 minutes, the reaction was diluted with EtOAc (300 mL) and washed with water (150 mL). The aqueous layer was extracted with EtOAc (300 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, concentrated in vacuo, dissolved in EtOH (50 mL) and water (5 mL) and then treated with p-toluenesulfonic acid monohydrate (5 mg). After stirring at 23° C. for 60 minutes, the solution was concentrated, dissolved in diethyl ether (300 mL) and washed with saturated NaHCO3 solution (100 mL), water (100 mL) and brine (100 mL), dried over MgSO4, and concentrated in vacuo affording 2.7 g of ethyl 3-(2-bromo-5-chlorophenyl)propiolate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928139B2
Source datasetuspto-grants-2011_04
ORD IDord-da7623e434804c49abe95a71d2a579b7
Source noteuspto-grants-2011_04