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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363362Generated: October 31, 2026

L-Proline → L-Alanyl-L-proline

https://huagongshe.com/reaction/2363362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ProlineHCID 145742—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
SolventWaterHCID 962—
ProductL-Alanyl-L-prolineHCID 83525—

Reaction Conditions

Temperature37 °C

Reaction Steps

L-Ala-OMe.HCl was added to the L-Pro-TBP prepared by the conversion of L-Pro into its ionic liquid form according to the method disclosed in Example 1 so as to control the concentration of the L-Ala-OMe.HCl to 1.000 mmol per unit mass (1 kg) of the L-Pro-TBP (the amount of water relative to the total mass of the reaction system: 2% by mass). The mixture was stirred enough to ensure the mixture uniform, and then, the reaction of these components was initiated while stirring the reaction system in a water bath and warming the same at 37° C. or 50° C. The reaction was finished 72 hours after the initiation of the reaction, and the samples, which were collected at appropriate intervals of time during the reaction, were analyzed according to the HPLC technique to confirm the formation of the desired dipeptide, i.e., L-Ala-Pro. The results are summarized in the following Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691941B2
Source datasetuspto-grants-2014_04
ORD IDord-8afda0efc9824386a0680113783bd5b5
Source noteuspto-grants-2014_04