Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127713Generated: October 24, 2026

Methanol → N-(Ethoxycarbonothioyl)-L-aspartic acid

https://huagongshe.com/en/reaction/127713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-Aspartic AcidHCID 5960—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl ethyl xanthateHCID 12515750—
SolventWaterHCID 962—
ProductN-(Ethoxycarbonothioyl)-L-aspartic acidHCID 5394491389%

Reaction Conditions

Temperature45 °C

Reaction Steps

L-Aspartic acid (19.95 g, 0.150 mol) was suspended in 15 ml of water at 0° C., and 50% sodium hydroxide solution (24 g, 0.30 mol) was added dropwise with stirring. Methyl ethyl xanthate (22.44 g, 0.165 mol) in 15 ml of methanol was then added in one portion. The mixture was heated at 45° C. for 2 hours, cooled to room temperature, and washed with two portions of ethylene dichloride. The ethylene dichloride washes were discarded and the aqueous phase acidified with concentrated hydrochloric acid at 0° C. The solution was saturated with solid sodium chloride and extracted with two portions of ethyl acetate. The organic extracts were dried over anhydrous magnesium sulfate and evaporated in vacuo to afford 29.4 g (89%) of white crystalline N-ethoxythiocarbonyl-L-aspartic acid. mp 133° C.; nmr (DMSO-d6) δ1.23 (t, 3H, J=7 Hz), 2.67 (d, 2H, J=6 Hz), 4.37 (q, 2H, J=7 Hz), 4.93 (dt, 1H, J=6 Hz, 8 Hz), 9.26 (d, 1H, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256897
Source datasetuspto-grants-1981_03
ORD IDord-202369a7eef443ae976c9ed556f237df
Source noteuspto-grants-1981_03