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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841137Generated: October 25, 2026

Triethylamine → Methyl 3-((2-(tert-butoxy)-2-oxoethyl)amino)propanoate

https://huagongshe.com/reaction/841137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantMethyl 3-aminopropanoate hydrochlorideHCID 2734767—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-((2-(tert-butoxy)-2-oxoethyl)amino)propanoateHCID 1484524514%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (7 mL, 50 mmol) was added to a solution of β-alanine methyl ester hydrochloride (5.25 g, 37.5 mmol) in methylene chloride (100 mL). The solution was cooled to 0° C. and t-butyl bromoacetate (4.88 g, 25 mmol) in methylene chloride (100 mL) was then added. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was removed in vacuo and the residue was taken up in ethyl acetate. The ethyl acetate was washed with saturated NaHCO3, brine, dried over MgSO4, filtered and concentrated in vacuo; 0.80 g (14% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369034B1
Source datasetuspto-grants-2002_04
ORD IDord-e51e580066c04d04b3613901de4d82bf
Source noteuspto-grants-2002_04