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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638544Generated: October 30, 2026

Iodoethane → HCID 20252626, compound

https://huagongshe.com/reaction/638544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTriethylamineHCID 8471—
ReactantHCID 20252638HCID 20252638—
SolventAcetonitrileHCID 6342—
ProductHCID 20252626HCID 2025262670%

Reaction Steps

31.2 g (0.2 mole) of ethyl iodide are added to a solution of 6.2 g (0.02 mole) of 5-(3,4-dichlorophenyl)-5-aminocarbonyl-1,2,3-oxathiazolidin-4-one-2-oxide and 2.02 g (0.02 mole) of triethylamine in 50 ml of acetonitrile. The solution is heated to the boil for four hours and then evaporated down under reduced pressure. The residue is taken up in 50 ml of dichloromethane, and the solution is washed with three times 20 ml of water. The organic phase is evaporated down and the residue is triturated with diethyl ether. In this manner, 4.7 g (70% of theory) of 3-ethyl-5-(3,4-dichlorophenyl)-5-aminocarbonyl-1,2,3-oxathiazolidin-4-one-2-oxide of melting point 127°-128° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562185
Source datasetuspto-grants-1985_12
ORD IDord-c790519ebc7642cf9c251bcef4ea63d7
Source noteuspto-grants-1985_12