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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186726Generated: October 26, 2026

Citric Acid → 8-acetoxy-4-(2-(diphenylmethoxy)ethyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/2186726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium hydrideHCID 24758—
Reactant[(2-Bromoethoxy)(phenyl)methyl]benzeneHCID 237821—
Reactant8-acetoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 22448941—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product8-acetoxy-4-(2-(diphenylmethoxy)ethyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 2244892366%

Reaction Steps

Anhydrous THF (15 ml) was added to sodium hydride (106 mg) to form a suspension, and a solution of 8-acetoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (498 mg) in anhydrous DMF (5 ml) was added to the resulting suspension, and the mixture was stirred at room temperature for 1 hour. 2-diphenylmethoxyethyl bromide (980 mg) was added to the mixture, and the mixture was stirred at room temperature overnight. The reaction solution was poured into a 3% citric acid aqueous solution, and then extracted with ethyl acetate. The resultant organic layer was washed with water and saturated brine, dried over sodium sulfate, and then concentrated. The residue was purified by medium-pressure column chromatography (solvent:ethyl acetate/cyclohexane=1/3) to obtain the colorless oily object compound (640 mg, yield 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407096B1
Source datasetuspto-grants-2002_06
ORD IDord-281571eacdd646c58c0ef5f734e216a5
Source noteuspto-grants-2002_06