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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260416Generated: October 30, 2026

Methanol → N-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanine

https://huagongshe.com/reaction/2260416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-PhenylalanineHCID 6140—
ReactantN-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamideHCID 11298025—
SolventWaterHCID 962—
ProductN-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanineHCID 92472—

Reaction Steps

The preparation of N-formyl-L-aspartic anhydride was repeated several times in order to prepare multiple first reaction mixtures. To each of these first reaction mixtures was added 100 ml of one of the alkyl ester or hindered alcohol solvents listed in Table 1 followed by the addition of 44.6 grams (0.27 mole) of L-phenylalanine. The resulting slurries were maintained at room temperature for 5 hours for completion of the in situ coupling process. As the reaction proceeded, the slurries became more and more solidified in each reaction and a quantity of a methanol and water solution (10:1) was added in order to dissolve all the solids therein. 2.0 grams aliquots were analyzed in each reaction mixture by HPLC. The resulting α/β ratios of N-formyl-L-aspartyl-L-phenylalanine formed in each reaction are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05476961
Source datasetuspto-grants-1995_12
ORD IDord-6b80c21a8e934dabb858a3d3d717bb88
Source noteuspto-grants-1995_12