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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502767Generated: November 3, 2026

Thiomorpholine → HCID 2732236, compound

https://huagongshe.com/reaction/502767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
Reactant4-Fluoro-3-nitrobenzotrifluorideHCID 67778—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2732236HCID 2732236—

Reaction Steps

To a solution of 1-fluoro-2-nitro-4-(trifluoromethyl)benzene (7.00 g, 33.48 mmol) in THF (250 ml) at room temperature was added thiomorpholine (3.45 g, 33.48 mmol) and sodium bicarbonate (3.66 g, 43.52 mmol). The vessel was purged with nitrogen and stirred at room temperature for 48 hours. After removal of solvent under reduced pressure, the mixture was taken up in ethyl acetate and filtered. The organics were washed with water, then brine and dried with magnesium sulfate. Filtration and concentration provided the title compound as a bright orange solid. MS m/z: 293.1 (M+H+); calc MW=292.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776869B2
Source datasetuspto-grants-2010_08
ORD IDord-527196c0086f444e8a4f38c52b1b7a6f
Source noteuspto-grants-2010_08