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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180085Generated: November 1, 2026

Triethylamine → Ethyl 3-(3-ethoxy-3-oxopropanamido)-3-methylbutanoate

https://huagongshe.com/reaction/1180085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
ReactantEthyl 3-amino-3-methylbutanoate hydrochlorideHCID 15578558—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(3-ethoxy-3-oxopropanamido)-3-methylbutanoateHCID 2519372197%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 3-amino-3-methylbutanoate hydrochloride (0.87 g, 4.79 mmol) was suspended on methylene chloride (12 mL) and triethylamine (1.4 mL, 2.1 eq.). The mixture was cooled to 0° C. and treated dropwise with ethyl 3-chloro-3-oxopropanoate (0.64 mL, 1.05 eq.). The reaction was kept at room temperature for 2 hours, diluted with methylene chloride, washed with 1 N HCl and then with 5% NaHCO3, dried over Na2SO4 and evaporated to dryness to obtain ethyl 3-[(3-ethoxy-3-oxopropanoyl)amino]-3-methylbutanoate (1.2 g, Y=97%) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279575B2
Source datasetuspto-grants-2007_10
ORD IDord-abf86e69b8eb4286999f3d6bf40a9578
Source noteuspto-grants-2007_10