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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839857Generated: October 31, 2026

Ethyl bromoacetate → 66935-31-7

https://huagongshe.com/reaction/839857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant2-MethoxyethylamineHCID 8018—
ReactantTriethylamineHCID 8471—
SolventBenzeneHCID 241—
Product66935-31-7HCID 1581881575.3%

Reaction Steps

To a stirred solution of 165.2 g of 2-methoxyethylamine and 202.4 g of triethylamine in 1 l of benzene was added dropwise a solution of 334.0 g of ethyl bromoacetate in 200 ml of benzene in one hour at room temperature. At the end of this period, the mixture was heated at reflux for 2 hours to complete the reaction. Upon chilling, the triethylamine hydrobromide was removed by filtration and washed with benzene. After removal of the solvent, the product was distilled in vacuo to yield 242.8 g (75.3 percent) of N-(2-methoxyethyl)glycine ethyl ester, B.P. 73°-5° C/4 mmHg. The following amino acid ethyl esters not previously reported in the chemical literature were synthesized by the aforementioned procedure which is essentially that as taught by A. J. Speziale et al., J. Org. Chem., 25 731 (1960).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097472
Source datasetuspto-grants-1978_06
ORD IDord-19e0ab8a6d49487e8d672ebd2a869732
Source noteuspto-grants-1978_06