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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13676Generated: October 25, 2026

Potassium Iodide → 2-Benzoyloxy-1,1-dimethoxy-ethane

https://huagongshe.com/reaction/13676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
Reactant2-Chloro-1,1-dimethoxyethaneHCID 60986—
ReactantPotassium BenzoateHCID 23661960—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Benzoyloxy-1,1-dimethoxy-ethaneHCID 1160817672.3%

Reaction Steps

Chloroacetaldehyde dimethyl acetal (50.0 g), potassium benzoate (70.7 g), potassium iodide (6.66 g) and DMF (N,N-dimethylformamide) (250 mL) were placed in a three-neck flask, followed by refluxing. Twenty hours later, the reaction mixture was cooled to room temperature, and water (250 mL) and ethyl acetate (250 mL) were added thereto, followed by stirring. After filtration, the filtrate was extracted with ethyl acetate (500 mL). The organic layer was subjected to vacuum concentration and then to vacuum distillation at 132-135° C. and at 5 mmHg and thereby yielded the target compound (61.0 g) in a yield of 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728152B2
Source datasetuspto-grants-2010_06
ORD IDord-fc9b9235d9cf49359251140b795631d9
Source noteuspto-grants-2010_06