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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751689Generated: October 28, 2026

Lithium Hydroxide → L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S)-

https://huagongshe.com/reaction/1751689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant(2S,5S)-ethyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-carboxylateHCID 67411636—
SolventMethanolHCID 887—
ProductL-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S)-HCID 6741268756%

Reaction Steps

(2S,5S)-Ethyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-carboxylate (39.3 mmol, assuming complete conversion from the previous transformation) was suspended in MeOH (200 mL) and aqueous LiOH (1.0 M, 100 mL, 100 mmol) was added. The reaction mixture was stirred o/n, then concentrated under reduced pressure to remove most of the MeOH. The aqueous solution was washed 2× with DCM before being acidified to pH˜1-2 with 10% HCl. The acidic aqueous phase was then extracted 5× with EtOAc. The combined EtOAc extracts were dried over MgSO4 filtered and concentrated under reduced pressure to afford (2S,5S)-1-((S)-2-(Methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-carboxylic acid (6.89 g, 56% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-b057c399fe144319aacc80545b6d73cd
Source noteuspto-grants-2015_10