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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920581Generated: October 30, 2026

Ethyl bromoacetate → HCID 67032460, compound

https://huagongshe.com/reaction/920581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 67032412HCID 67032412—
SolventAcetonitrileHCID 6342—
ProductHCID 67032460HCID 6703246087%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 2-[4-(2,6-dichloro-benzyloxy)-phenyl]-morpholine hydrochloride (0.65 g; 1.68 mmol), Et3N (0.58 mL; 4.2 mmol), and ethyl bromoacetate (0.24 ml; 2.19 mmol) in CH3CN (65 mL) was stirred at 85° C., overnight. After cooling to RT the mixture was concentrated in vacuo and the residue partitioned between water and CH2Cl2. The layers were separated and aqueous layer was extracted once more with CH2Cl2. The combined organic layers were concentrated in vacuo and the residue was purified by column chromatography (SiO2, Et2O:hexanes 2:1) to afford {2-[4-(2,6-dichloro-benzyloxy)-phenyl]-morpholin-4-yl}-acetic acid ethyl ester (0.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-09abfe6a42324688ad7b7825f340c53e
Source noteuspto-grants-2016_03