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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56094Generated: October 29, 2026

Triethylamine → 4-(2-Fluoro-4-nitrophenyl)thiomorpholine

https://huagongshe.com/reaction/56094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThiomorpholineHCID 67164—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventEthyl AcetateHCID 8857—
Product4-(2-Fluoro-4-nitrophenyl)thiomorpholineHCID 1082407172.2%

Reaction Steps

To a solution of thiomorpholine (3.57 g, 34.56 mmol) and Et3N (3.50 g, 34.56 mmol) in EtOAc was added 3,4-difluoronitrobenzene (5.00 g, 31.43 mmol) dropwise over a period of 30 min in an ice bath. Upon the end of addition the reaction mixture was warmed to rt slowly, and solid was precipitated out. The mixture was filtered. The filter cake was washed with an appropriate amount of water, dried in vacuo to obtain the 1st crop of product. The filtrate was extracted with EtOAc. The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo to obtain the 2nd crop of product. The solids of 1st crop and 2nd crop were combined to give the title compound as a yellow solid (5.50 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-198e6cfb0c8c40b490dbd50204ff5491
Source noteuspto-grants-2016_09