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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166334Generated: October 26, 2026

4-(Methylsulfonyl)aniline → HCID 178491240, compound

https://huagongshe.com/reaction/1166334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)anilineHCID 79617—
Reactant3-Fluoro-4-methoxybenzonitrileHCID 2774548—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178491240HCID 178491240—

Reaction Steps

To a suspension of 4-(methylsulfonyl)aniline (2.82 g, 16.5 mmol) in toluene (150 mL), trimethylaluminum (2M solution in toluene, 12.5 mL, 24.7 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 3-fluoro-4-methoxybenzonitrile (5 g, 33 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture was heated to 80-85° C. After 20 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol (2/1). The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more hexane/ether (2/1). The pale yellow solid 3-fluoro-4-methoxy-N-(4-(methylsulfonyl)phenyl]benzenecarboximidamide (3.95 g, 74%) was used in the next reaction without further purification: mp (DSC) 195C. Anal. Calc'd. for C15H15N2SO3F: C, 55.89, H, 4.69, N, 8.69. Found: C, 55.92, H, 4.74, N, 8.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613789B2
Source datasetuspto-grants-2003_09
ORD IDord-94e1651d96374ff69e3c1e4799125a38
Source noteuspto-grants-2003_09