Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175714Generated: November 2, 2026

Dimethyl Sulfoxide → (Z)-ethyl 4-(2-iodo-4,5-dimethoxybenzamido)but-2-enoate

https://huagongshe.com/reaction/2175714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(2-hydroxyethyl)-2-iodo-4,5-dimethoxybenzamideHCID 67087759—
SolventDichloromethaneHCID 6344—
Product(Z)-ethyl 4-(2-iodo-4,5-dimethoxybenzamido)but-2-enoateHCID 7093555234%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of dry DMSO (0.453 mL, 6.4 mmol) in DCM (2 mL) was added dropwise to a solution of oxalyl chloride (0.338 mL, 4 mmol) in DCM (5 mL) at −78° C. The reaction was stirred for 30 min at −78° C. then a solution of N-(2-hydroxyethyl)-2-iodo-4,5-dimethoxybenzamide (702 mg, 2 mmol) in DCM (3 mL) was added via cannula. The mixture was stirred at −78° C. for 1 hour then dry Et3N (1.7 mL, 12 mmol) was added slowly. Stirring was continued at −78° C. for 1 hour by which time the formation of the aldehyde was complete (monitored by TLC). Solid Ph3P═CHCOOEt (1.0 g, 3 mmol) was then added and the reaction was allowed to warm slowly to room temperature overnight. The solvent was removed under reduced pressure and the crude product was purified by flash column using petroleum ether/ethyl acetate (from 6:1 to 3:1) as eluent to give (Z)-ethyl 4-(2-iodo-4,5-dimethoxybenzamido)but-2-enoate (280 mg, 34%). LC-MS (ES-API); rt 8.46 min; m/z calculated for C15H18INO5 [M+H]+ 420.0, found 420.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-8b115c159e084d088222a97a04ae4bf7
Source noteuspto-grants-2015_06