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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl propiolate | HCID 12182 | — |
| Reactant | 1,2-Difluoro-4-iodobenzene | HCID 2724444 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,4-Difluoro-phenyl)-propynoic acid ethyl ester | HCID 58312680 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344161B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-6529e96bffbc4c32bd3111f3c9bcba43 |
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| Source note | uspto-grants-2013_01 |
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