Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007937Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 22666363, compound

https://huagongshe.com/reaction/1007937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantHCID 22666419HCID 22666419—
SolventEthyl AcetateHCID 8857—
ProductHCID 22666363HCID 22666363—

Reaction Conditions

Temperature60 °C

Reaction Steps

In 59 mL of dimethyl sulfoxide is dissolved 11.8 g of methyl 2,4-difluoro-3-methoxybenzoate, to which are added 23.0 g of potassium carbonate and 9.33 g of sodium hydrogen sulfide n-hydrate (purity 70%). The mixture is stirred at 60° C. for 2 hours. Then, 25 mL of bromoacetaldehyde diethyl acetal is added at the same temperature as above, and stirred at that temperature for 3 hours. Water and ethyl acetate are added to the reaction mixture, and the organic layer is separated. The organic layer is washed with saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue is purified by column chromatography (eluent: hexane-ethyl acetate=5:1) to obtain 19.0 g of methyl 4-[(2,2-diethoxyethyl)sulfanyl]-2-fluoro-3-methoxybenzoate as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-2bfd42948f504af8b6276efad3e6f060
Source noteuspto-grants-2004_09