Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-Chloro-3-fluoropyridine | HCID 2782791 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-3-fluoro-4-iodopyridine | HCID 11065087 | 54.4% |
Reaction Steps
A solution of lithium diisopropylamide (2M in tetrahydrofuran/ethylbenzene/heptane, 155 mL, 0.31 mol) was added dropwise over 40 minutes to solution of 2-chloro-3-fluoropyridine (31 g, 0.235 mol) in tetrahydrofuran (200 mL) at −70° C. and the resulting mixture stirred for 4 hours. A solution of iodine (69 g, 0.2 mol) in tetrahydrofuran (100 mL) was added dropwise over 30 minutes and the resultant mixture was stirred for 30 minutes at −70° C. then allowed to warm to room temperature over 1 hour. The reaction mixture was poured onto aqueous sodium metabisulphite solution (20% w/v, 2 L) and extracted with diethyl ether (3×300 mL). The combined organic extract was washed with aqueous sodium metabisulphite solution (20% w/v, 2 L) and water (200 mL), dried over Na2SO4 and evaporated under reduced pressure to give a colorless oil. The resultant oil was triturated with diethyl ether to give the desired compound as a red/brown solid (28 g, 46% yield). 1H NMR (400 MHz, CDCl3): δ 7.87 (d, J=5.0 Hz, 1H), 7.66 (ddd, J=5.0, 4.0, 0.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697708B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-9d37aa9dd2be4f5b80e1a907b1204964 |
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| Source note | uspto-grants-2014_04 |
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