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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167898Generated: November 1, 2026

Ethyl bromoacetate → HCID 67032460, compound

https://huagongshe.com/reaction/2167898

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 numberUS09045441B2
Source datasetuspto-grants-2015_06
ORD IDord-7a94749acc3f43f89c840c84638474ff
Source noteuspto-grants-2015_06