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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669857Generated: October 31, 2026

1,3-Dichloro-5-iodobenzene → 1,3-Dichloro-5-ethynylbenzene

https://huagongshe.com/reaction/1669857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-5-iodobenzeneHCID 76424—
ReactantHCID 178418486HCID 178418486—
CatalystZinc bromideHCID 10421208—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product1,3-Dichloro-5-ethynylbenzeneHCID 13823547—

Reaction Steps

To a solution of zinc bromide (5.0 g, 22.2 mmol) in anhydrous THF (100 mL) at room temperature under a nitrogen atmosphere was added a solution of ethynyl magnesium bromide (0.5 M in THF, 44.4 mL, 44.4 mmol). After 5 minutes 3,5-dichloro-iodobenzene was added (4.03 g, 14.8 mmol) followed by tetrakis-triphenyl phosphine palladium (0) (855 mg, 0.74 mmol). The reaction was stirred at room temperature for 18 hours. The reaction mixture was poured into brine and extracted with ether (4×100 mL). The ether layer was washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography with hexanes to give the title compound as a yellow solid. 1H NMR (CDCl3, 500 MHz): δ 7.4 (d, J=1.6 Hz, 2H), 7.3 (d, J=1.6 Hz, 1H), 3.19 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989475B2
Source datasetuspto-grants-2011_08
ORD IDord-f8456564c6c743b9bc595e63a5041f9e
Source noteuspto-grants-2011_08