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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527228Generated: October 31, 2026

Methyl 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoate → Potassium 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoate

https://huagongshe.com/reaction/527228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoateHCID 66617968—
ReactantHCID 178504318HCID 178504318—
SolventTetrahydrofuranHCID 8028—
ProductPotassium 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoateHCID 66617918105%

Reaction Steps

Methyl 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoate (133 g, 374 mmol) was dissolved in THF (1.0 L) and treated with KOTMS (56.0 g, 392 mmol) at room temperature. The mixture was allowed to stir overnight to completion by LCMS analysis of the crude. The mixture was concentrated in vacuo to afford a wet foam, which was allowed to dry under vacuum overnight to afford potassium 3-(tert-butoxycarbonyl(isopropyl)amino)-2-(4-chlorophenyl)propanoate as a white solid (148.7 g, 105%). LC/MS (APCI+) m/z 242.1 [M-Boc-K]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346789B2
Source datasetuspto-grants-2016_05
ORD IDord-df06dfa28ddb4e26aaad5d9092c11d5e
Source noteuspto-grants-2016_05