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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254539Generated: October 25, 2026

Dimethyl Sulfoxide → 2-Chloro-6-iodobenzaldehyde

https://huagongshe.com/reaction/254539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(2-Chloro-6-iodophenyl)methanolHCID 58951679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Chloro-6-iodobenzaldehydeHCID 589518911,037.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3.11 ml (36.2 mmol) oxalyl chloride in 40 ml dichloromethane at −78° C. was added dropwise over 20 min a solution of 5.14 ml (72.4 mmol) dimethylsulfoxide in 15 ml dichloromethane. The mixture was stirred for a further 15 min at −78° C. and then a solution of 8.10 g (3.02 mmol) (2-chloro-6-iodo-phenyl)-methanol in 40 ml dichloromethane was added dropwise over 30 min and stirring continued at −78° C. for a further 45 min. 20.9 ml (151 mmol) triethylamine were then added dropwise and the reaction mixture allowed to warm to room temperature. Water was then added and the phases were then separated. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo to afford 8.35 g (100%) of the title compound as a yellow crystalline solid which was used in the next step without further purification. MS (EI): 268.0 (44%) & 266.0 (100%) (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875645B2
Source datasetuspto-grants-2011_01
ORD IDord-7ea4857795b04740af63a9116ce4be6d
Source noteuspto-grants-2011_01