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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236044Generated: October 25, 2026

L-Phenylalanine, methyl ester → L-Phenylalanine, L-alpha-aspartyl-, 2-methyl ester, hydrochloride (1:1)

https://huagongshe.com/reaction/236044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Phenylalanine, methyl esterHCID 736234—
ReactantChloroacetyl l-aspartic acid anhydrideHCID 53642311—
SolventAcetic AcidHCID 176—
Solvent1,1-DichloroethaneHCID 6365—
ProductL-Phenylalanine, L-alpha-aspartyl-, 2-methyl ester, hydrochloride (1:1)HCID 13460048%

Reaction Conditions

Temperature-5 °C

Reaction Steps

150 Grams of N-chloroacetyl-L-aspartic acid anhydride are quickly added, at -5° C., to the solution of 140 grams of methyl L-phenylalaninate in 400 ml of dichloroethane plus 200 ml of acetic acid. The mixture is stirred for 1 hour at -5° C.; the temperature is then raised, in 2 hours, to 15° C., then, in 30 minutes, to 40° C. The dichloroethane is evaporated under vacuum; 500 ml of methanol and 60 grams of thiourea are added and the mixture is refluxed for 3 hours. After cooling to 20° C., 200 ml of methanol, containing 11% (by weight) of HCl, are added, the solution is cooled to 0° C. for 1 hour, filtered and evaporated to dryness in vacuo. The residue is crystallized from 600 ml of water containing 70 g of NaCl: a very pure aspartame hydrochloride is obtained, in a 48% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642367
Source datasetuspto-grants-1987_02
ORD IDord-47bb1c994bc54a1096b3d379686c6f2f
Source noteuspto-grants-1987_02