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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230213Generated: October 27, 2026

Hydrochloride methanol → (S)-tert-Butyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochloride

https://huagongshe.com/reaction/2230213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
Reactanttert-Butyl (2S)-benzyloxycarbonylamino-3-tert-butoxycarbonylaminopropionateHCID 53876012—
CatalystPalladiumHCID 23938—
Product(S)-tert-Butyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochlorideHCID 8658573399%

Reaction Steps

13.1 g of tert-butyl (S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonylaminopropionate were hydrogenated over 10% Pd/C in methanol/HCl. After 1.5 h, the mixture was filtered and the filtrate was concentrated in vacuo. 9.77 g (99%) of tert-butyl (S)-2-amino-3-tert-butoxycarbonylaminopropionate hydrochloride were obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423712B1
Source datasetuspto-grants-2002_07
ORD IDord-5cd0063416f4469f846e0ad623b3f16c
Source noteuspto-grants-2002_07