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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085624Generated: November 3, 2026

Hydrochloric Acid → 5-oxothiomorpholine-3-carboxylic Acid

https://huagongshe.com/reaction/1085624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoacetamideHCID 3727—
ReactantSodium CarbonateHCID 10340—
ReactantL-Cysteine hydrochloride monohydrateHCID 23462—
SolventWaterHCID 962—
Product5-oxothiomorpholine-3-carboxylic AcidHCID 3556697—

Reaction Steps

A solution of 1.75 g (10 mmole) of L-cysteine hydrochloride monohydrate dissolved in 50 ml of water was adjusted to pH 8.0 with 1M sodium carbonate. Under nitrogen gas stream, 1.85 g (10 mmole) of monoiodoacetamide and 1M sodium carbonate were added alternately while maintaining pH at 8.0. After the reaction was carried out at room temperature for 1 hour, further the reaction was carried out in a sealed tube at 100° C. for 2 hours. To the reaction mixture was added 4N HCl to adjust the pH to 3.25, followed by concentration to dryness. The residue was extracted with hot ethanol, and after cooling, the crystals were collected by filtration and recrystallized from hot ethanol. Yield: 560 mg (34.8%), melting point: 182° to 184° C., Fab mass analysis [M+H]+= 162.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010174
Source datasetuspto-grants-1991_04
ORD IDord-5f73d798f8ad4b57a89f9a7d3d9c9788
Source noteuspto-grants-1991_04