HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52297Generated: October 24, 2026
Dichloromethane → 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide
https://huagongshe.com/en/reaction/52297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | 4-(Methylsulfonyl)benzonitrile | HCID 519981 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide | HCID 178504763 | 35% |
Reaction Steps
To a suspension of 4-fluoroaniline (4 mL, 40 mmol) in toluene (120 mL), trimethylaluminum (2M solution in toluene, 21 mL, 42 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 3 hours. A solution of 4-(methylsulfonyl)benzonitrile (7.65 g, 40 mmol) in methylene chloride (100 mL) was added over 10 minutes and the reaction mixture was heated to 70°-75° C. After 48 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. The combined filtrates were concentrated in vacuo and the resulting crude intermediate (7.7 g) was chromatographed [silica gel, hexane/ethyl acetate, 25/75] to give 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide (4.1 g, 35%) as a white solid: mp (DSC) 182° C. Anal. Calc'd. for C14H13N2SO2F: C, 57.52, H, 4.48, N, 9.58, S, 10.97. Found: C, 57.37, H, 4.69, N, 9.21, S, 10.69.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616601 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-79d9344789514a02b4037e46ddef742f |
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| Source note | uspto-grants-1997_04 |
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