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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923992Generated: October 30, 2026

Potassium Hydroxide → 2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid

https://huagongshe.com/reaction/1923992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDiethyl 2-((tert-butoxycarbonyl)amino)malonateHCID 382219—
SolventWaterHCID 962—
SolventWater ethanolHCID 19096565—
Product2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acidHCID 11011022—

Reaction Steps

To a solution of 1,3-diethyl 2-{[(tert-butoxy)carbonyl]amino}propanedioate XCVI (2.22 g, 8 mmol) in a mixture of ethanol/water (45 mL/5 mL) was added KOH (0.45 g, 8 mmol) in water (3 mL) dropwise. The reaction mixture was stirred for 1.5 hours. The ethanol was evaporated and the residue was acidified to pH=2 by 2 M HCl and washed by DCM. The organic layer was washed with brine and dried over MgSO4. The solvent was evaporated to give 2-{[(tert-butoxy)carbonyl]amino}-3-ethoxy-3-oxopropanoic acid XCVII as crystals (1.68 g, 6.8 mmol, 85% yield). 1H NMR (CDCl3) 1.31 (t, J=7 Hz, 3H), 1.41-1.45 (m, 9H), 4.23-4.31 9 m, 2H), 4.76 (d, J=4 Hz, 1H), 7.77 (d, J=4 Hz, 1H), 10.84 (brs, 1H); ESIMS found for C10H17NO6 m/z 248 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178490B2
Source datasetuspto-grants-2012_05
ORD IDord-513c80883a7b4ca497e2be56435f9217
Source noteuspto-grants-2012_05