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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868366Generated: October 29, 2026

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/868366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-PhenylalanineHCID 6140—
ReactantAspartameHCID 134601—
ReactantN-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamideHCID 11298025—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHydrochloric AcidHCID 313—
ProductN-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanineHCID 92472—
ProductAspartameHCID 134601—

Reaction Steps

The present invention relates to a process for preparing α-L-aspartyl-L-phenylalanine methyl ester or its hydrochloride. α-L-aspartyl-L-phenylalanine methyl ester or its hydrochloride is prepared by a process comprising: condensating N-formyl-L-aspartic acid anhydride and L-phenylalanine in water or in water containing methanol at a pH in the range of 7-12 to form N-formyl-α-L-aspartyl-L-phenylalanine; acidifying the reaction mixture successively with hydrochloric acid in the presence of methanol without isolating the N-formyl-α-L-aspartyl-L-phenylalanine so as to bring it into contact with hydrochloric acid in the presence of methanol for reaction and thereby to deposit α-L-aspartyl-L-phenylalanine methyl ester hydrochloride; separating the α-L-aspartyl-L-phenylalanine methyl ester hydrochloride; and neutralizing said hydrochloride as required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778916
Source datasetuspto-grants-1988_10
ORD IDord-539e94da77a349f2973308e2a06070ff
Source noteuspto-grants-1988_10