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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675844Generated: 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/1675844

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 numberUS08003651B2
Source datasetuspto-grants-2011_08
ORD IDord-cf11f1bed46e4b6a87dbb33b89a3eb77
Source noteuspto-grants-2011_08