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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244051Generated: November 1, 2026

Ethyl bromoacetate → HCID 69654916, compound

https://huagongshe.com/reaction/1244051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantHCID 21931738HCID 21931738—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
ProductHCID 69654916HCID 69654916126.7%

Reaction Steps

A mixture of 0.28 g (0.73 mmol) 3-benzenesulfonylmethyl-6-[1,3]dioxolan-2-yl-5-methoxy-2-nitro-pyridine and 0.8 ml (0.73 mmol) of ethyl bromoacetate was dissolved in 10 ml of ethanol. To this solution was added 0.5 ml of potassium t-butoxide (1M in t-butyl alcohol) and the reaction mixture was stirred at room temperature for 1 hour. The solvent was evaporated and the residue was added to 5 ml of water. The suspension was extracted with ethyl acetate. The ethyl acetate extract was dried (Na2SO4) and evaporated to yield approximately 0.3 g of an oil. Mass spectrum: m/e=325.1 (p+1). This material was used directly in step 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119207B2
Source datasetuspto-grants-2006_10
ORD IDord-a8725e3c7a07468183cb7c4f45eb4126
Source noteuspto-grants-2006_10