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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799771Generated: November 1, 2026

Ethyl propiolate → (3,4-Difluoro-phenyl)-propynoic acid ethyl ester

https://huagongshe.com/reaction/1799771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl propiolateHCID 12182—
Reactant1,2-Difluoro-4-iodobenzeneHCID 2724444—
ReactantLithium diisopropylamideHCID 2724682—
CatalystZinc bromideHCID 10421208—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(3,4-Difluoro-phenyl)-propynoic acid ethyl esterHCID 58312680—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under argon atmosphere, a four neck flask was charged with THF (135 ml) and 2 M LDA in THF (60.9 ml, 0.12 mol, 1.18 eq.) and cooled to −78° C. Propynoic acid ethyl ester (12.2 g, 0.12 mol, 1.18 eq.) dissolved in THF (36 ml) was added dropwise within 30 min. Then, ZnBr2 (28.5 g, 0.12 mol, 1.2 eq.) dissolved in THF (45 ml) was added dropwise within 30 min. After the addition of 1,2-Difluoro-4-iodo-benzene (25.0 g, 0.10 mol) and tetrakis(triphenylphosphine) palladium(0) (6.02 g, 5.15 mmol, 5 mol %), the reaction mixture was allowed to warm to r.t. and stirred for another 3 h at the same temperature. The reaction mixture was diluted with diethylether and washed with saturated aqueous NH4I, saturated aqueous NaHCO3 and brine. The organic phase was dried with Na2SO4, concentrated under reduced pressure and dried under vacuum. The residue was purified by silica gel filtration (heptane/ethyl acetate 98:2) to yield 16.6 g (76%) of Vc as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344161B2
Source datasetuspto-grants-2013_01
ORD IDord-6529e96bffbc4c32bd3111f3c9bcba43
Source noteuspto-grants-2013_01