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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896114Generated: October 30, 2026

Thiomorpholine → 4-(2,6-Difluoro-4-nitrophenyl)thiomorpholine

https://huagongshe.com/reaction/896114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2,3-Trifluoro-5-nitrobenzeneHCID 2782793—
SolventAcetonitrileHCID 6342—
Product4-(2,6-Difluoro-4-nitrophenyl)thiomorpholineHCID 12096592—

Reaction Steps

A solution of 3,4,5-trifluoronitrobenzene (5.00 g, 28.24 mmol) in acetonitrile (60 mL) is cooled to 0° C. and treated with N,N-diisopropylethylamine (7.38 mL, 42.35 mmol) followed by thiomorpholine (2.98 mL, 29.65 mmol). The ice bath is removed and the reaction mixture stirred at room temperature under nitrogen for approximately 24 h, during which additional thiomorpholine (0.1 eq) is added. The solvent is removed under reduced pressure, and the residue is diluted with ethyl acetate, washed with 1N hydrochloric acid (until the washings are acidic), saturated aqueous sodium bicarbonate and saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound, mp 104-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919329B2
Source datasetuspto-grants-2005_07
ORD IDord-49a6800b262043928cdb8445e17fd0f0
Source noteuspto-grants-2005_07