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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

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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538004B2
Source datasetuspto-grants-2003_03
ORD IDord-8be7e6f840834857af7f0bcd7c59c9ca
Source noteuspto-grants-2003_03