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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682079Generated: November 2, 2026

Phosphate → HCID 86746434, compound

https://huagongshe.com/reaction/1682079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantEthyl vinyl etherHCID 8023—
ReactantDimercaptosuccinic AcidHCID 9354—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86746434HCID 86746434—

Reaction Steps

A solution of meso 2,3-dimercaptosuccinic acid (4.55 g, 25 mmol) in 50 mL dichloromethane or tetrahydrofuran or other similar aprotic solvents containing p-toluenesulfonic acid monohydrate (0.048 g, 0.252 mmol) is cooled to -18° to -25° C. with constant stirring. Ethyl vinyl ether (4.8 mL, 50 mmol) in 50 mL dichloromethane or other aprotic solvents is added dropwise to the cold solution over a period of 1.5 to 2 hours. The stirring is continued for an additional 30 minutes with the temperature maintained in the -18° to -25° C. range. Then 20 mL of pH 7 phosphate buffer is added, and the reaction mixture is allowed to warm with stirring for 10 to 15 minutes. The reaction mixture is then poured into a flask containing 100 mL of ethyl acetate and 25 mL of deionized water. The layers are separated and the aqueous portion is extracted three times, each time with 50 mL ethyl acetate. The organic layers are combined, washed with water and then brine. The washed ethyl acetate extract is then dried over anhydrous sodium sulfate. Removal of the solvent gives 2 to 3 g of bis S-(1-ethoxyethyl) 2,3-dimercaptosuccinic acid. The material is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175256
Source datasetuspto-grants-1992_12
ORD IDord-4c41e790cd1842ffb9da058e485f1a3b
Source noteuspto-grants-1992_12