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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114391Generated: October 31, 2026

Trifluoroacetic acid → HCID 57488859, compound

https://huagongshe.com/reaction/2114391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant6-methoxy-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 13204952—
SolventTetrahydrofuranHCID 8028—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 57488859HCID 5748885960%

Reaction Steps

A solution of 6-(methyloxy)-2H-1,4-benzoxazin-3(4H)-one (2.08 g, 11.6 mmol) dissolved in 12.5 mL of anhydrous tetrahydrofuran was added drop-wise to a mixture of sodium hydride (60% by weight in mineral oil, 0.52 g, 12.8 mmol) suspended in 25 mL of anhydrous tetrahydrofuran under argon. The mixture was allowed to stir at room temperature for 10 minutes and then ethyl bromoacetate (1.54 mL, 13.9 mmol) was added to the mixture and stirred vigorously for 1.5 hours before it was determined to be complete by LCMS (two Aquasil C18, 20×1 mm columns were run in sequence, 4 minutes at 0.1 mL/min, 1-99% CH3CN/H2O with 0.018% trifluoroacetic acid, ES) Rt=1.5 min and m/e 265 [M+1]+. The reaction was quenched by adding 5 mL of a 4 M solution of hydrochloric acid in dioxane. After allowing the mixture to stir for one hour, all of the volatiles were removed by rotary evaporation, and the crude residue was purified by silica gel chromatography (120 g Redisep column, silica, 40 um, 60 Å, 50 mL/min, A: methylene chloride, B: methanol, B: 10% for 5 min, 80% for 30 min; detection at 214 nm) to give ethyl [6-(methyloxy)-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetate (1.82 g, 6.9 mmol, 60%). MS (ES) m/e 265 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-efb1b0ff0ae84c7892afe2d8aeb7e1c0
Source noteuspto-grants-2008_10