HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862412Generated: November 2, 2026
Potassium Sodium Tartrate → 3-Iodo-4-methylbenzaldehyde
https://huagongshe.com/reaction/1862412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Iodo-4-methylbenzoic acid | HCID 621640 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Product | 3-Iodo-4-methylbenzaldehyde | HCID 12330254 | 30.8% |
Reaction Steps
3-Iodo-4-methyl-benzoic acid (1.0 g, 3.96 mmol) in dry CH2Cl2:THF 1:1 (200 mL) was treated with oxalyl chloride (1 mL, 11.9 mmol) and several drops of DMF. The mixture was heated at 65° C. for 30 minutes, cooled to ambient temperature, and concentrated under reduced pressure to provide a light yellow solid. The obtained solid in THF (200 mL) was treated with LiAlH(OtBu)3 (4.1 mL, 4.1 mmol) via syringe at −78° C. After 30 minutes at −78° C., a saturated solution of Rochelle's salt was added and the mixture was allowed to warm to ambient temperature. The organic layer was washed in succession with 1 NHCl, saturated NaHCO3, brine, dried over Na2SO4, and the solvent removed under reduced pressure. The resulting residue was purified by flash chromatography using hexanes:EtOAc (4:1) as eluent to provide 3-iodo-4-methylbenzaldehyde as a white solid (300 mg, 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06538004B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-8be7e6f840834857af7f0bcd7c59c9ca |
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| Source note | uspto-grants-2003_03 |
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