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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221214Generated: October 31, 2026

Ethyl bromoacetate → HCID 13204948, compound

https://huagongshe.com/reaction/221214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, 4-methoxy-2-nitro-HCID 15285—
SolventAcetoneHCID 180—
ProductHCID 13204948HCID 13204948—

Reaction Steps

A mixture of 4-methoxy-2-nitrophenol 9 (1.69 g, 0.01 mol), potassium carbonate (2.76 g, 0.02 mol) and ethyl bromoacetate 6d (1.1 mL, 0.01 mol) in 20 mL anhydrous acetone was refluxed for overnight (12 h). The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was evaporated, the residue was diluted with water and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and evaporated to give ethyl 2-(4-methoxy-2-nitrophenoxy)acetate 11 which was purified by silica gel column chromatography using 0-50% gradient of hexane and ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207163B2
Source datasetuspto-grants-2012_06
ORD IDord-5d4227879d9b4480b81e0490b2b60295
Source noteuspto-grants-2012_06