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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789910Generated: October 29, 2026

Water → 2-[1-(6-tert-Butoxycarbonylamino-pyridin-3-yl)-2-methyl-propyl]-malonic acid monoethyl ester

https://huagongshe.com/reaction/1789910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant2-[1-(6-Tert-butoxycarbonylamino-pyridin-3-yl)-2-methyl-propyl]-malonic acid diethyl esterHCID 54326381—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product2-[1-(6-tert-Butoxycarbonylamino-pyridin-3-yl)-2-methyl-propyl]-malonic acid monoethyl esterHCID 54331446—

Reaction Steps

To a solution of 2-[1-(6-tert-butoxycarbonylamino-pyridin-3-yl)-2-methyl-propyl]-malonic acid diethyl ester (1.569 g, 3.84 mmol) in a mixture of dichloromethane (6 mL) and ethanol (12 mL, 95%) at 0° C. a solution of potassium hydroxide (0.272 g, 85%, 4.2 mmol) in ethanol (6 mL, 95%) was added dropwise over 40 min. After additional 1 h stirring the mixture was allowed to warm up to room temperature and stirring was continued for 18 h. Then water (30 mL) and dichloromethane (30 mL) were added, and after 3 min stirring the layers were separated. The organic was extracted once with water and the combined aqueous were washed once with ether. Then an aqueous solution of citric acid (10%) was added to adjust the pH to 4, and the solution was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulphate. After evaporation of the solvent crude 2-[1-(6-tert-butoxycarbonylamino-pyridin-3-yl)-2-methyl-propyl]-malonic acid monoethyl ester (0.94 g, 64%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071175B1
Source datasetuspto-grants-2006_07
ORD IDord-531d900b1a5549609a8857c78e89db2d
Source noteuspto-grants-2006_07