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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369811Generated: October 31, 2026

Ethanol → 3-(3-pentyl)-L-phenylalanine

https://huagongshe.com/reaction/369811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(2R,3S,5S)-oxo-2,3-diphenyl-5-(3-(3-pentyl)benzyl)morpholineHCID 57269594—
CatalystPalladium ChlorideHCID 24290—
SolventTetrahydrofuranHCID 8028—
Product3-(3-pentyl)-L-phenylalanineHCID 2063768384%

Reaction Steps

To a 300 mL Parr bottle were added 0.41 g of PdCl2, 1.36 g of (2R, 3S, 5S)-6-oxo-2,3-diphenyl-5-(3-(3-pentyl)benzyl)morpholine, 50 mL of EtOH, and 30 mL of THF. The mixture was deoxygenated by bubbling nitrogen through for 10 min and was hydrogenated at 45 psi for 18 h. The vessel was purged with nitrogen, catalyst removed by filtration through celite, and the filtrate concentrated in vacuo to a volume of 15 mL. The solution was chilled in an ice bath and triturated with additional of 50 mL of hexane. A fine precipitate slowly formed. After storing at 5° C. overnight, the solid was collected by filtration and dried in vacuo to afford 0.65 g (72%) of 3-(3-pentyl)-L-phenylalanine.HCl as a white powder, m.p. 170° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140100
Source datasetuspto-grants-2000_10
ORD IDord-dba9e60ecb8e446aa2010cb0b1633f22
Source noteuspto-grants-2000_10