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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459589Generated: November 3, 2026

Methane, dichloromethoxy- → 5-Iodo-2-methoxybenzaldehyde

https://huagongshe.com/reaction/1459589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantChlorineHCID 24526—
Reactant4-IodoanisoleHCID 69676—
ReactantSodium BicarbonateHCID 516892—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product5-Iodo-2-methoxybenzaldehydeHCID 262240—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2.04 grams (8.72 mmol) of 4-iodoanisole in 36 mL of CH2Cl2, cooled to 0° C., was added dropwise 2.0 mL (18.7 mmol) of titanium tetrachloride. After stirring for 30 min., 0.93 mL (10.3 mmol) of α,α-dichloromethyl methyl ether was added and the reaction maintained at 0° C. for another 2 hours. The reaction mixture was then poured with stirring into a mixture of 50 mL of CH2 Cl2 and 50 mL of saturated aqueous sodium bicarbonate (NaHCO3). After 30 min., this was filtered through diatomaceous earth, the organic layer was separated, the aqueous layer was twice extracted with CH2 Cl2, and all of the organic layers were combined, dried with MgSO4 and concentrated in vacuo. The crude residue was recrystallized from ethanol (EtOH) to give 5-iodo-2-methoxybenzaldehyde as pale yellow needles, 1.37 grams (60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854262
Source datasetuspto-grants-1998_12
ORD IDord-fcb1255ff61c493a83f2869a138d11ef
Source noteuspto-grants-1998_12