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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Iodo-4-methylbenzoic acidHCID 621640—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
Product3-Iodo-4-methylbenzaldehydeHCID 1233025430.8%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780872B2
Source datasetuspto-grants-2004_08
ORD IDord-978831c3f1d84dec8a1e9d05455b6240
Source noteuspto-grants-2004_08