HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 5-Fluoro-3-(3-p-toluenesulfonyloxypropyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 3-(5-fluoro-1H-indol-3-yl)propan-1-ol | HCID 15020541 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Fluoro-3-(3-p-toluenesulfonyloxypropyl)indole | HCID 15020542 | 79% |
Reaction Steps
To a stirred solution of 3-(5-fluoro-1H-indol-3-yl)-propan-l-ol (2.90 g, 15.0 mmol) in pyridine (15.0 mL) was added p-toluenesulfonyl chloride (7.1 g, 37.5 mmol) at room temperature. After stirring for 30 minutes at room temperature, the reaction mixture was poured to 200 nm of ice water. The aqueous was extracted with ethyl acetate and the combined organic extracts were washed with IN HCI and brine. The resulting material was dried over anhydrous sodium sulfate, filtered, and the solvent was concentrated under vacuum. The crude product was purified by silica gel column chromatography (ethyl acetatehexane, 3n) to give 4.1 g (79%) of the title compound as a solid: mp 74 CC (Lit. mp 99 ° C.; EP 464604 A2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06291683B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-ac37f212a5d84d8ebf7481c256366770 |
| Source note | uspto-grants-2001_09 |