Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245218Generated: November 1, 2026

Acetic Acid → Ac-D-Lys-D-Pro-D-Val-NH2

https://huagongshe.com/reaction/2245218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantAc-D-Lys(Z)-D-Pro-D-Val-NH2HCID 131727991—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductAc-D-Lys-D-Pro-D-Val-NH2HCID 986483098.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

107 g of Ac-D-Lys(Z)-D-Pro-D-Val-NH2 are dissolved in 535 ml of EtOH, added with 214 ml of AcOH and of 21.4 g of Pd/C at 10% at 50% water. The hydrogenation is conducted at 20° C., under a 1 bar hydrogen pressure for 16 hours. The reaction completion is CCM controlled. The catalyst is filtered and the filtrate is vacuum concentrated until refusal. The residue is recovered with 107 ml of EtOH, added with 430 ml of iPrOH and the blend is heated at 50° C., then added dropwise at 50° C. with 1500 ml of diisopropyl ether. The expected product crystallizes. The medium is cooled down to 20° C. and stirred for 1 hour. The solid is filtered and washed with 500 ml of diisopropyl ether before being vacuum dried at 25° C. so to provide 78.3 g of Ac-D-Lys-D-Pro-D-Val-NH2 under the form of an acetate salt (yield 85.4%). The thus obtained product purity is HPLC controlled.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683026B2
Source datasetuspto-grants-2010_03
ORD IDord-3310000f698543cbb4a583dcd431bf6b
Source noteuspto-grants-2010_03