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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625747Generated: October 30, 2026

4-Methylmorpholine → Benzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylate

https://huagongshe.com/reaction/625747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-(4-Fluorophenyl)oxazolidine-2,5-dioneHCID 86649049—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylateHCID 1143888864.1%

Reaction Steps

To a solution of 4-(4-fluorophenyl)oxazolidine-2,5-dione (2.5 g, 12.8 mmol) in THF (30 mL) cooled to −25° C. was added benzyl chloroformate (2.3 mL, 16.6 mmol), followed by the slow addition (˜10 min) of N-methylmorpholine (2.11 mL, 19.2 mmol) as a solution in THF (5 mL). The solution was stirred at this temperature for 1 h. and then allowed to warm to rt overnight. The resulting solution was filtered through Celite, and the filtrate was concentrated. The resulting crude material was recrystallized from 2:2:1 t-butyl methyl ether:hexanes:THF to give benzyl 4-(4-fluorophenyl)-2,5-dioxooxazolidine-3-carboxylate (2.7 g, 64%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308207B2
Source datasetuspto-grants-2016_04
ORD IDord-0d89d39743bb41238d6a0d06399a9d11
Source noteuspto-grants-2016_04