HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560943Generated: October 30, 2026
Iodine → 3-Fluoro-4-iodo-1,1'-biphenyl-2-carbonitrile
https://huagongshe.com/reaction/560943
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-Cyano-3-fluorobiphenyl | HCID 23509652 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Fluoro-4-iodo-1,1'-biphenyl-2-carbonitrile | HCID 66680937 | — |
Reaction Steps
A solution of Example 243A (6.8 g, 34.5 mmol) in THF (110 mL) at −78° C. under nitrogen atmosphere was treated dropwise with LDA (2.0 M solution in THF) and stirred for 1 h, then a solution of iodine in THF (30 mL) was added via cannula over about 10 min. The thick mixture was allowed to warm to rt and stirred for 1 h, then treated with saturated aqueous Na2SO3 solution (10 mL). The mixture was concentrated to remove the THF, then H2O was added and the mixture was extracted with EtOAc. The extracts were washed with brine, dried (MgSO4) and concentrated. The residue was purified by flash chromatography on silica gel, eluting with EtOAc/hexanes (1:7), and the resulting solid was triturated with hexanes and EtOAc to give the desired product (6.8 g). Rf=0.44 (7:1 hexane:EtOAc)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063091B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-1fe70c5a5acb44488659c2a8d8e66952 |
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| Source note | uspto-grants-2011_11 |
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