HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102245Generated: October 30, 2026
1,3-Dichloro-5-iodobenzene → 1,3-Dichloro-5-ethynylbenzene
https://huagongshe.com/reaction/2102245
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dichloro-5-iodobenzene | HCID 76424 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 1,3-Dichloro-5-ethynylbenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572922B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-8f701a7564bf41b19ef0100cdef22c1a |
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| Source note | uspto-grants-2009_08 |
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