HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 10425834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-(Methylsulfonyl)aniline | HCID 79617 | — |
| Reactant | 3-(1,3-Dioxolan-2-yl)-1-(4-fluorophenyl)-1-propanone | HCID 2758696 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10425834 | HCID 10425834 | 55% |
Reaction Steps
A mixture of the ketone (Step 2) (448 mg, 2 mmol), 4-(methylsulfonyl)aniline (380 mg, 2.2 mmol) and p-toluenesulfonic acid (30 mg) in toluene (40 ml) was heated to reflux for 18 hours. The reaction was cooled, filtered and concentrated. The crude solid (750 mg) was purified by chromatography (silica gel, hexane/ethyl acetate, 1/1) to give 2-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-pyrrole (310 mg, 55%) as a white solid: mp (DSC) 201° C. Anal Calc'd. for C17H14NSFO2 ·0.2 H2O: C, 64.01; H, 4.55; N, 4.39; S, 10.05. Found: C, 64.18; H, 4.33; N, 4.32; S, 10.36.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935990 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-0d89e49363a64769bedf1b7368e05842 |
| Source note | uspto-grants-1999_08 |