HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245282Generated: October 30, 2026
Dimethylformamide → 2-Fluoro-6-iodobenzaldehyde
https://huagongshe.com/reaction/2245282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1-Fluoro-3-iodobenzene | HCID 70725 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-6-iodobenzaldehyde | HCID 11096976 | 100.2% |
Reaction Steps
Buthyllithium (1.6 M, 60 ml, 0.113 mol) is added to an ice cooled solution of diisopropyl-amine (17.6 ml, 0.124 mol) in THF (200 ml). The solution is stirred at 0° C. for 30 minutes and is cooled to −78° C. 1-Fluoro-3-iodo-benzene (25 g, 0.113 mol) in THF (20 ml) is slowly added to the preformed LDA mixture. The resulting solution is stirred for another hour after which DMF (9.55 ml, 0.124 mol) is added and stirring is continued for another 30 minutes at −78° C. The reaction is quenched first with acetic acid (20 ml) followed by water (200 ml). The mixture is extracted with ether. The organic layer is washed with a 2N HCl solution, brine, is dried over MgSO4 and evaporated to afford the desired compound (28.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683075B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9d012ab647574a73b5aa93397c2114a7 |
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| Source note | uspto-grants-2010_03 |
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