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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788678Generated: November 3, 2026

Hydrochloric Acid → HCID 56629638, compound

https://huagongshe.com/reaction/1788678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantD-ThreonineHCID 69435—
Reactant3-(Methylsulphonyl)-2-oxoimidazolidine-1-carbonyl chlorideHCID 3016299—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 56629638HCID 5662963856.3%

Reaction Steps

D-Threonine (5.0 g) was suspended in water (50 ml) and treated with 2M aqueous sodium hydroxide solution to pH 10, forming a clear solution. The pH was then re-adjusted to 7.5 with concentrated hydrochloric acid and the still clear solution cooled to 15°. 3-Methanesulphonyl-2-oxoimidazolidine-1-carbonyl chloride (9.5 g) was then added portionwise over 2 minutes, with simultaneous addition of 2M aqueous sodium hydroxide to maintain the pH at 6.0-7.5. Following this, acetone (30 ml) was added to give a clear solution which was then stirred at room temperature for 1 hour whilst still maintaining the pH at 6.0-7.5. After evaporation of the acetone in vacuo the aqueous residue was extracted well with ethyl acetate and the organic extracts were discarded. The pH of the aqueous phase was then adjusted to 1.5 with concentrated hydrochloric acid and the mixture was extracted using 3×50 ml portions of ethyl acetate:tetrahydrofuran (1:1). The organic extracts were dried and the solvent was evaporated to give the title compound as a white solid, (7.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684641
Source datasetuspto-grants-1987_08
ORD IDord-cdb7f170466e44ea945ffad42c2724c9
Source noteuspto-grants-1987_08