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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114370Generated: November 1, 2026

Trifluoroacetic acid → HCID 57488853, compound

https://huagongshe.com/reaction/2114370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant7-Methoxy-2H-1,4-benzoxazin-3(4H)-oneHCID 11600770—
SolventTetrahydrofuranHCID 8028—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 57488853HCID 5748885364.6%

Reaction Steps

A solution of 7-(methyloxy)-2H-1,4-benzoxazin-3(4H)-one (1.42 g, 7.9 mmol) dissolved in 5 mL of anhydrous THF was added to a suspension of sodium hydride (0.349 g of a 60% dispersion in mineral oil, 8.7 mmol) in 10 mL of anhydrous THF at room temperature and stirred for 10 minutes. Then, ethyl bromoacetate (1.06 mL, 9.52 mmol) was added and stirred at room temperature for two hours. HPLC (Eclipse XDB-C18, 4.6×250 mm, 5 micron, 1-99% CH3CN/H2O with 0.1% trifluoroacetic acid) showed that all of the starting material (Rt=4.4 min) was gone and that a new peak (Rt=6.5 min) had formed. The reaction was quenched with 5 mL of 4.0M HCl in dioxane. The solvent was removed by rotary evaporation and the residue was adsorbed onto approximately 10 g of silica gel and purified by column chromatography (120 g silica gel 40 um, gradient elution from 100% dichloromethane to 10% methanol/90% dichloromethane over 40 minutes) to give ethyl [7-(methyloxy)-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetate (1.35 g, 5.1 mmol, 64%) as a white crystalline solid. MS (ES) m/e 266 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-8b160b2919c6490b8c97417fafcf87cc
Source noteuspto-grants-2008_10