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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657166Generated: October 28, 2026

Ethyl bromoacetate → HCID 178516869, compound

https://huagongshe.com/reaction/657166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68484103HCID 68484103—
SolventEthanolHCID 702—
ProductHCID 178516869HCID 178516869—

Reaction Steps

To a suspension of 4-amino-2-[(E)-2-phenylethenyl]-5-pyrimidinol hydrochloride (250 mg, 1.0 mmol) in absolute ethanol (5 mL) was added potassium tert-butoxide (224 mg, 2.0 mmol) at room temperature. After stirring for 5 minutes, ethyl bromoacetate (0.11 mL, 1.0 mmol) was added via dropwise addition and the reaction was stirred for 18 h. The solvent was evaporated and the residue was taken up in 10% MeOH—CHCl3 and a small amount of water. The layers were separated and the aqueous phase was extracted with 10% MeOH—CHCl3 (3×). The combined organic extracts were concentrated and the resulting solid was triterated with EtOAc. The white solid was collected by filtration, yielding 106 mg (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-8ff8ed0bf62d41b49fc2f3108df8325e
Source noteuspto-grants-2011_12