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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583896Generated: October 25, 2026

Phosphorus trichloride → N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester

https://huagongshe.com/reaction/1583896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
ReactantL-Phenylalanine, methyl esterHCID 736234—
ReactantN-acetoacetyl-L-aspartic anhydrideHCID 13334674—
ReactantDisodium N-acetoacetylaspartateHCID 86739332—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductN-acetoacetyl-L-aspartyl-L-phenylalanine methyl esterHCID 13334676—

Reaction Steps

Crude disodium N-acetoacetylaspartate, 28.51 parts, was stirred with 200 parts by volume of ethyl acetate and 11.7 parts by volume of acetic acid at 0°-5° C. under argon while 4.37 parts by volume of phosphorous trichloride was added dropwise. The resulting mixture was allowed to warm to ambient temperatures while stirring for 20 hours. To the resulting solution which contains N-acetoacetyl-L-aspartic anhydride was added dropwise over a 2 hour period 122 parts by volume of 0.9M L-phenylalanine methyl ester in dioxane. After continued stirring for 20 hours, the solvent was evaporated under vacuum at 35°-40° C. Toluene, 200 parts by volume, was added to the residue and the evaporation was repeated, giving crude N-acetoacetyl-L-aspartyl-L-phenylalanine methyl ester as a semi-solid yellow residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04555362
Source datasetuspto-grants-1985_11
ORD IDord-6ab30196dcec42a59680382c5d2f7837
Source noteuspto-grants-1985_11