HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837056Generated: November 1, 2026
Potassium Sodium Tartrate → 3-Iodo-4-methylbenzaldehyde
https://huagongshe.com/reaction/1837056
Participants
| Role | Name | HCID | Charge |
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| 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 1N HCl, 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 | US06780872B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-978831c3f1d84dec8a1e9d05455b6240 |
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| Source note | uspto-grants-2004_08 |
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